Sharekhan

Zydus Lifesciences Ltd

Tue 29/04/2025,15:59:4 | NSE : ZYDUSLIFE

₹ 888.051.50 (0.17%)

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Market Data

Essential tool: analyze, trade, manage, decide.

Open

₹ 887.00

Previous Close

₹ 886.55

Volume

1027694

Mkt Cap ( Rs. Cr)

₹89358.61

High

₹ 894.85

Low

₹ 877.05

52 Week High

₹ 1324.30

52 Week Low

₹ 795.00

Book Value Per Share

₹ 216.89

Dividend Yield

0.33

Face Value

₹ 1.00

What’s Your Call?

Collective community sentiment on Zydus Lifesciences Ltd

Your Vote -

Buy

71.19%

Hold

16.71%

Sell

12.10%

71.19%

7146 users have voted

Market Depth

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Buy Order Quantity

0%

Sell Order Quantity

100%

Bid Price

Qty

0.00

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Bid Total

0

Bid Price

Qty

888.05

117

0.00

0

0.00

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Bid Total

117

Option Chain

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News

Media spotlight triggers stock stock attention, sentiment.

  • Zydus Lifesciences - Announcement under Regulation 30 (LODR)-Press Release / Media Release

    26 Apr 2025, 9:54AM Closure of USFDA inspection at Zydus' API Unit at Dabhasa, Gujarat.
  • Zydus Lifesciences - Press Release

    26 Apr 2025, 9:52AM Zydus Lifesciences Limited has informed the Exchange regarding a press release dated April 26, 2025, titled ""Closure of USFDA inspection at Zydus AP
  • Zydus Lifesciences - Press Release

    25 Apr 2025, 9:33PM Zydus Lifesciences Limited has informed the Exchange regarding a press release dated April 25, 2025, titled ""Zydus Lifesciences Limited signs purchas
  • Zydus Lifesciences - Announcement under Regulation 30 (LODR)-Press Release / Media Release

    25 Apr 2025, 9:32PM Press Release
  • Zydus Lifesciences - Announcement under Regulation 30 (LODR)-Updates on Acquisition

    25 Apr 2025, 9:30PM Zydus Lifesciences Limited signs purchase agreement with PAI Partners and other shareholders to acquire a majority stake in Amplitude SA
  • Zydus Lifesciences - General Updates

    25 Apr 2025, 9:29PM Zydus Lifesciences Limited has informed the Exchange about General Updates
  • Zydus Lifesciences - Press Release

    17 Apr 2025, 7:47PM Zydus Lifesciences Limited has informed the Exchange regarding a press release dated April 17, 2025, titled ""Zydus Medtech and Braile Biomedica of Br
  • Zydus Lifesciences - Announcement under Regulation 30 (LODR)-Press Release / Media Release

    17 Apr 2025, 7:44PM Press Release
  • Zydus Lifesciences - Pendency of Litigation(s)/dispute(s) or the outcome impacting the Company

    17 Apr 2025, 3:36PM Zydus Lifesciences Limited has informed the Exchange about Pendency of Litigation(s)/dispute(s) or the outcome impacting the Company
  • Zydus Lifesciences - Press Release

    17 Apr 2025, 11:30AM Zydus Lifesciences Limited has informed the Exchange regarding a press release dated April 17, 2025, titled ""Zydus Lifesciences Limited announces the
  • Zydus Lifesciences - News Verification

    17 Apr 2025, 9:39AM The Exchange has sought clarification from Zydus Lifesciences Limited with respect to recent news item captioned Lupin, Zydus Life shares fall up to 5
  • Zydus Lifesciences - Announcement under Regulation 30 (LODR)-Press Release / Media Release

    17 Apr 2025, 11:50AM Zydus Lifesciences Limited announces the execution of undertakings to tender as part of its envisaged tender offer for Amplitude Surgical SA shares.
  • Zynext Ventures Invests in Feldan Therapeutics to Advance Intracellular Drug Delivery

    17 Apr 2025, 10:28AM Zynext Ventures USA LLC, the venture capital arm of Zydus Lifesciences, has announced a strategic investment in Feldan Therapeutics, a Canada-based ea
  • Zydus Lifesciences - Announcement under Regulation 30 (LODR)-Press Release / Media Release

    16 Apr 2025, 9:12PM Zynext Ventures Invests in Feldan Therapeutics to Drive Innovation in Intracellular Drug Delivery.
  • Zydus Lifesciences - Press Release

    16 Apr 2025, 9:09PM Zydus Lifesciences Limited has informed the Exchange regarding a press release dated April 16, 2025, titled ""Zynext Ventures Invests in Feldan Therap
  • Zydus Lifesciences - Rumour verification - Regulation 30(11)

    16 Apr 2025, 7:06PM Clarification
  • Zydus Lifesciences - Rumour Verification - Regulation 30(11)

    16 Apr 2025, 7:04PM Zydus Lifesciences Limited has informed the Exchange about Rumour Verification - Regulation 30(11)
  • Zydus Lifesciences - Clarification/Confirmation On News Item Appearing In \Www.Cnbctv18.Com\

    16 Apr 2025, 6:45PM Clarification
  • Zydus Lifesciences - News Verification

    16 Apr 2025, 3:49PM The Exchange has sought clarification from Zydus Lifesciences Limited with respect to recent news item captioned Lupin, Zydus Life shares fall up to 5
  • Zydus Lifesciences - Clarification sought from Zydus Lifesciences Ltd

    16 Apr 2025, 4:05PM The Exchange has sought clarification from Zydus Lifesciences Ltd on April 16, 2025, with reference to news appeared in www.cnbctv18.com dated April 1
  • Zydus Lifesciences has submitted to BSE the Shareholding Pattern for the Period Ended March 31, 2025

    12 Apr 2025, 7:00PM As of March 2025, 75.00% is owned by Indian Promoters and 25.01% by Public. <p align=justify> Institutional holds 18.31% (Insurance Companies 4.38%) a
  • Zydus Lifesciences - Incorporation-XBRL

    12 Apr 2025, 4:53PM ZYDUS LIFESCIENCES LIMITED has informed the Exchange regarding Incorporation
  • Zydus Lifesciences - Press Release

    11 Apr 2025, 9:38PM Zydus Lifesciences Limited has informed the Exchange regarding a press release dated April 11, 2025, titled ""Zydus receives final approval from USFDA
  • Zydus Lifesciences - Announcement under Regulation 30 (LODR)-Press Release / Media Release

    11 Apr 2025, 9:33PM Zydus received final approval from USFDA for Jaythari (Deflazacort) Tablets, 6 mg, 18 mg, 30 mg, and 36 mg
  • Zydus Lifesciences - General Updates

    11 Apr 2025, 6:44PM Zydus Lifesciences Limited has informed the Exchange about General Updates
  • Zydus Lifesciences - Incorporation Of A Wholly Owned Subsidiary In France

    11 Apr 2025, 6:40PM Incorporation of a wholly owned subsidiary in France
  • Zydus Lifesciences - Certificate under SEBI (Depositories and Participants) Regulations, 2018

    9 Apr 2025, 11:47AM Zydus Lifesciences Limited has informed the Exchange about Certificate under SEBI (Depositories and Participants) Regulations, 2018
  • Zydus Lifesciences - Compliances-Certificate under Reg. 74 (5) of SEBI (DP) Regulations, 2018

    9 Apr 2025, 11:50AM Certificate under regulation 74(5) of the SEBI (Depositories and Participants) Regulations, 2018
  • Zydus Lifesciences - Update-Acquisition/Scheme/Sale/Disposal-XBRL

    28 Mar 2025, 7:06PM ZYDUS LIFESCIENCES LIMITED has informed the Exchange regarding Update-Acquisition/Scheme/Sale/Disposal-XBRL
  • Zydus Lifesciences - Announcement under Regulation 30 (LODR)-Updates on Acquisition

    28 Mar 2025, 6:46PM Update on acquisition of a business
  • Zydus Lifesciences - General Updates

    28 Mar 2025, 6:44PM Zydus Lifesciences Limited has informed the Exchange about General Updates
  • Zydus Lifesciences - Copy of Newspaper Publication

    28 Mar 2025, 2:03PM Zydus Lifesciences Limited has informed the Exchange about Copy of Newspaper Publication
  • Zydus Lifesciences - Trading Window-XBRL

    25 Mar 2025, 5:10PM ZYDUS LIFESCIENCES LIMITED has informed the Exchange about Closure of Trading Window
  • Zydus Lifesciences - Trading Window

    25 Mar 2025, 5:03PM Zydus Lifesciences Limited has informed the Exchange regarding the Trading Window closure pursuant to SEBI (Prohibition of Insider Trading) Regulation
  • Zydus Lifesciences - Press Release

    18 Mar 2025, 5:07PM Zydus Lifesciences Limited has informed the Exchange regarding a press release dated March 18, 2025, titled ""Zydus receives final approval from USFDA
  • Zydus Lifesciences - Announcement under Regulation 30 (LODR)-Press Release / Media Release

    18 Mar 2025, 5:09PM Zydus receives final approval from USFDA for Apalutamide Tablets, 60 mg.
  • Zydus secures USFDA approval for Eluxadoline Tablets (75 mg & 100 mg)

    17 Mar 2025, 9:56AM Zydus Lifesciences Limited, along with its subsidiaries and affiliates, has received final approval from the U.S. Food and Drug Administration (USFDA)
  • Zydus Lifesciences - Press Release

    16 Mar 2025, 2:09PM Zydus Lifesciences Limited has informed the Exchange regarding a press release dated March 16, 2025, titled ""Zydus receives final approval from USFDA
  • Zydus Lifesciences - Announcement under Regulation 30 (LODR)-Press Release / Media Release

    16 Mar 2025, 2:12PM Zydus receives final approval from USFDA for Eluxadoline Tablets, 75 mg and 100 mg.
  • Zydus Lifesciences - Press Release

    14 Mar 2025, 11:18PM Zydus Lifesciences Limited has informed the Exchange regarding a press release dated March 14, 2025, titled ""Closure of USFDA inspection at Zydus AP
  • Zydus Lifesciences - Copy of Newspaper Publication

    13 Mar 2025, 1:58PM Zydus Lifesciences Limited has informed the Exchange about Copy of Newspaper Publication
  • Zydus Lifesciences - Announcement under Regulation 30 (LODR)-Press Release / Media Release

    12 Mar 2025, 8:35PM Zynext Ventures invests in Illexcor Therapeutics to advance novel oral therapy for sickle cell disease.
  • Zydus Lifesciences - Press Release

    12 Mar 2025, 8:32PM Zydus Lifesciences Limited has informed the Exchange regarding a press release dated March 12, 2025, titled ""Zynext Ventures invests in Illexcor Ther
  • Zydus Lifesciences - Press Release

    12 Mar 2025, 12:53PM Zydus Lifesciences Limited has informed the Exchange regarding a press release dated March 12, 2025, titled ""Zydus receives final approval from USFDA
  • Zydus Lifesciences - Announcement under Regulation 30 (LODR)-Press Release / Media Release

    12 Mar 2025, 12:56PM Zydus receives final approval from USFDA for Methenamine Hippurate Tablets USP, 1 gram.
  • Zydus Lifesciences - Acquisition-XBRL

    11 Mar 2025, 5:45PM ZYDUS LIFESCIENCES LIMITED has informed the Exchange regarding Acquisition
  • Zydus Lifesciences - Investor Presentation

    11 Mar 2025, 5:01PM Zydus Lifesciences Limited has informed the Exchange about Investor Presentation
  • Zydus Lifesciences - Analysts/Institutional Investor Meet/Con. Call Updates

    11 Mar 2025, 2:34PM Zydus Lifesciences Limited has informed the Exchange about Schedule of meet
  • Zydus Lifesciences - Outcome of Board Meeting

    11 Mar 2025, 1:21PM Zydus Lifesciences Limited has informed the Exchange regarding Outcome of Board Meeting held on March 11, 2025.
  • Zydus Lifesciences - Announcement under Regulation 30 (LODR)-Acquisition

    11 Mar 2025, 1:21PM Acquisition of shares of Amplitude Surgical SA, France, a listed entity
  • Zydus Lifesciences - Announcement under Regulation 30 (LODR)-Investor Presentation

    11 Mar 2025, 5:03PM Investor presentation
  • Zydus Lifesciences - Announcement under Regulation 30 (LODR)-Analyst / Investor Meet - Intimation

    11 Mar 2025, 2:37PM Investor Conference
  • Zydus Lifesciences to acquire majority stake in Amplitude Surgical for &euro;256.8 mn

    11 Mar 2025, 2:36PM Zydus Lifesciences announced on Tuesday that it has entered into exclusive negotiations to acquire a majority stake in France-based Amplitude Surgical
  • Zydus Lifesciences - Press Release

    10 Mar 2025, 9:38AM Zydus Lifesciences Limited has informed the Exchange regarding a press release dated March 10, 2025, titled ""Zydus receives final approval from USFDA
  • Zydus receives USFDA approval for Ketoconazole Shampoo 2%

    10 Mar 2025, 12:32PM Zydus Lifesciences Limited has secured final approval from the U.S. Food and Drug Administration (USFDA) to manufacture and market Ketoconazole Shampo
  • Zydus Lifesciences - Announcement under Regulation 30 (LODR)-Press Release / Media Release

    10 Mar 2025, 9:41AM Zydus receives final approval from USFDA for Ketoconazole Shampoo, 2%.
  • Zydus Lifesciences - Copy of Newspaper Publication

    8 Mar 2025, 1:42PM Zydus Lifesciences Limited has informed the Exchange about Copy of Newspaper Publication
  • Zydus Lifesciences - Updates

    5 Mar 2025, 4:00PM Zydus Lifesciences Limited has informed the Exchange regarding 'Revised ESG Score'.
  • Zydus Lifesciences - Press Release

    5 Mar 2025, 3:46PM Zydus Lifesciences Limited has informed the Exchange regarding a press release dated March 05, 2025, titled ""Zydus receives final approval from USFDA
  • Zydus Lifesciences - Press Release

    5 Mar 2025, 9:41AM Zydus Lifesciences Limited has informed the Exchange regarding a press release dated March 05, 2025, titled ""Zydus Lifesciences launches ANVIMO, a br
  • Zydus Lifesciences - Revised ESG Score

    5 Mar 2025, 4:02PM Revised ESG Score
  • Zydus Lifesciences - Announcement under Regulation 30 (LODR)-Press Release / Media Release

    5 Mar 2025, 3:50PM Zydus receives approval from USFDA for Dasatinib Tablets, 20 mg, 50 mg, 70 mg, 80 mg, 100 mg, and 140 mg.
  • Zydus Lifesciences launches ANVIMO, a breakthrough in transplant care

    5 Mar 2025, 9:57AM Zydus Lifesciences, a global discovery-based life sciences company, has introduced ANVIMO (Letermovir), a groundbreaking solution for preventing Cytom
  • Zydus Lifesciences - Announcement under Regulation 30 (LODR)-Press Release / Media Release

    5 Mar 2025, 9:44AM Zydus Lifesciences launches ANVIMO, a breakthrough for transplant patients Made-in-India for India, ANVIMO brings access and affordability.
  • Zydus Lifesciences - Press Release

    4 Mar 2025, 10:45AM Zydus Lifesciences Limited has informed the Exchange regarding a press release dated March 04, 2025, titled ""Zydus, supported by the Gates Foundation
  • Zydus pioneers World&rsquo;s First Typhoid-Shigella combination vaccine with Gates Foundation Support

    4 Mar 2025, 11:17AM Zydus Lifesciences Limited, a global innovation-driven life sciences company, has announced its groundbreaking initiative to develop the world&rsquo;s
  • Zydus Lifesciences - Announcement under Regulation 30 (LODR)-Press Release / Media Release

    4 Mar 2025, 10:49AM Zydus, supported by the Gates Foundation, to develop the world's first combination vaccine to offer protection against shigellosis and typhoid for inf
  • Zydus Lifesciences - Action(s) taken or orders passed

    3 Mar 2025, 9:48AM Zydus Lifesciences Limited has informed the Exchange about Action(s) taken or orders passed
  • Zydus Lifesciences - Demand Notice Received By Zydus Healthcare Limited, A Wholly Owned Subsidiary Company, From GST Departme

    3 Mar 2025, 9:52AM Demand notice received by Zydus Healthcare Limited, a wholly owned subsidiary company, from GST department
  • Zydus Lifesciences - Press Release

    26 Feb 2025, 10:55AM Zydus Lifesciences Limited has informed the Exchange regarding a press release dated February 26, 2025, titled ""Zydus Lifesciences- first in India to
  • Zydus Lifesciences - Announcement under Regulation 30 (LODR)-Press Release / Media Release

    26 Feb 2025, 10:58AM Zydus Lifesciences- first in India to launch protection against new strain of influenza virus (Southern Hemisphere 2025).
  • Zydus Lifesciences - Press Release

    22 Feb 2025, 11:56AM Zydus Lifesciences Limited has informed the Exchange regarding a press release dated February 22, 2025, titled ""Zydus receives final approval from US
  • Zydus Lifesciences - Announcement under Regulation 30 (LODR)-Press Release / Media Release

    22 Feb 2025, 11:59AM Zydus receives final approval from USFDA for Ibuprofen and Famotidine Tablets, 800 mg/26.6 mg.
  • Zydus Lifesciences - Analysts/Institutional Investor Meet/Con. Call Updates

    19 Feb 2025, 9:49AM Zydus Lifesciences Limited has informed the Exchange about Schedule of meet
  • Zydus Lifesciences - Announcement under Regulation 30 (LODR)-Analyst / Investor Meet - Intimation

    19 Feb 2025, 9:52AM The Company is going to participate in IIFL's 16th Enterprising India Global Investors' Conference at Mumbai on Wednesday, February 26, 2025.
  • Zydus Lifesciences - Announcement under Regulation 30 (LODR)-Press Release / Media Release

    14 Feb 2025, 5:13PM Closure of USFDA inspection at Zydus' API manufacturing plant at Ambernath, Maharashtra.
  • Zydus Lifesciences - Press Release

    14 Feb 2025, 5:10PM Zydus Lifesciences Limited has informed the Exchange regarding a press release dated February 14, 2025, titled ""Closure of USFDA inspection at Zydus
  • Zydus Lifesciences - Announcement under Regulation 30 (LODR)-Press Release / Media Release

    14 Feb 2025, 3:08PM Zydus and Beihai Biotech sign an exclusive licensing, supply and commercialization agreement for BEIZRAY (Albumin Solubilized Docetaxel Injection), a
  • Zydus Lifesciences - Press Release

    14 Feb 2025, 3:04PM Zydus Lifesciences Limited has informed the Exchange regarding a press release dated February 14, 2025, titled ""Zydus and Beihai Biotech sign an excl
  • Zydus Lifesciences - Announcement under Regulation 30 (LODR)-Press Release / Media Release

    14 Feb 2025, 12:55PM Stock exchange intimation on closure of USFDA inspection at Zydus' topical plant.
  • Zydus Lifesciences - Press Release

    14 Feb 2025, 12:52PM Zydus Lifesciences Limited has informed the Exchange regarding a press release dated February 14, 2025, titled ""Stock Exchange intimation on closure
  • Zydus Lifesciences - Press Release

    12 Feb 2025, 4:02PM Zydus Lifesciences Limited has informed the Exchange regarding a press release dated February 12, 2025, titled ""Zydus and Synthon sign an exclusive d
  • Zydus Lifesciences - Analysts/Institutional Investor Meet/Con. Call Updates

    12 Feb 2025, 9:57AM Zydus Lifesciences Limited has informed the Exchange about Schedule of meet
  • Zydus Lifesciences - Announcement under Regulation 30 (LODR)-Press Release / Media Release

    12 Feb 2025, 4:05PM Zydus and Synthon sign an exclusive development, licensing, supply and commercialization agreement for a novel 505(B)(2) oncology product for the US m
  • Zydus Lifesciences - Announcement under Regulation 30 (LODR)-Analyst / Investor Meet - Intimation

    12 Feb 2025, 10:01AM The Company is going to participate in an investor conference 'Kotak: CHASING GROWTH 2025' at Mumbai on Thursday, February 20, 2025
  • Zydus Lifesciences - Announcement under Regulation 30 (LODR)-Earnings Call Transcript

    11 Feb 2025, 6:29PM Transcript of the post results earnings call held on February 5, 2025
  • Zydus Lifesciences - Analysts/Institutional Investor Meet/Con. Call Updates

    11 Feb 2025, 6:24PM Zydus Lifesciences Limited has informed the Exchange about Transcript
  • Zydus Lifesciences - Change in Directors/ Key Managerial Personnel/ Auditor/ Compliance Officer/ Share Transfer Agent

    11 Feb 2025, 12:53PM ZYDUS LIFESCIENCES LIMITED has informed the Exchange about Change in Directors/ Key Managerial Personnel/ Auditor/ Compliance Officer/ Share Transfer
  • Zydus Lifesciences - Change in Management

    10 Feb 2025, 1:10PM Zydus Lifesciences Limited has informed the Exchange about change in Management
  • Zydus Lifesciences - Announcement under Regulation 30 (LODR)-Change in Management

    10 Feb 2025, 1:07PM Changes in Senior Management
  • Zydus Lifesciences - Copy of Newspaper Publication

    6 Feb 2025, 2:01PM Zydus Lifesciences Limited has informed the Exchange about Copy of Newspaper Publication
  • Zydus Lifesciences - Intimation Of ESG Rating

    6 Feb 2025, 12:14PM Intimation of ESG Rating
  • Zydus Lifesciences - Updates

    6 Feb 2025, 12:12PM Zydus Lifesciences Limited has informed the Exchange regarding 'Intimation of ESG Rating'.
  • Zydus Lifesciences - Analysts/Institutional Investor Meet/Con. Call Updates

    5 Feb 2025, 10:13PM Zydus Lifesciences Limited has informed the Exchange about Link of Recording
  • Zydus Lifesciences - Integrated Filing- Financial

    5 Feb 2025, 12:50PM Integrated Filing- Financial
  • Zydus Lifesciences - Press Release

    5 Feb 2025, 12:33PM Zydus Lifesciences Limited has informed the Exchange regarding a press release dated February 05, 2025, titled ""Press Release"".
  • Zydus Lifesciences - Announcement under Regulation 30 (LODR)-Press Release / Media Release

    5 Feb 2025, 12:33PM Press Release relating to unaudited financial results for the quarter / nine months ended on December 31, 2024
  • Zydus Lifesciences - Investor Presentation

    5 Feb 2025, 12:28PM Zydus Lifesciences Limited has informed the Exchange about Investor Presentation
  • Zydus Lifesciences - Financial Result Updates

    5 Feb 2025, 12:23PM Zydus Lifesciences Limited has submitted to the Exchange, the financial results for the period ended December 31, 2024.
  • Zydus Lifesciences - Integrated Filing (Financial)

    5 Feb 2025, 12:48PM Integrated Filing (Financial) for the quarter / nine months ended December 31, 2024
  • Zydus Lifesciences Q3 net profit up 4.48% at Rs 470.60 cr

    5 Feb 2025, 12:31PM The company reported standalone net profit of Rs 470.60 crore for the quarter ended December 31, 2024 as compared to Rs 450.40 crore in the same perio
  • Zydus Lifesciences - Announcement under Regulation 30 (LODR)-Investor Presentation

    5 Feb 2025, 12:31PM Investor Presentation
  • Zydus Lifesciences - Board Meeting Outcome for Unaudited Financial Results For The Quarter / Nine Months Ended On December 31

    5 Feb 2025, 12:29PM Unaudited financial results for the quarter / nine months ended on December 31, 2024
  • Zydus Lifesciences - Unaudited Financial Results For The Quarter / Nine Months Ended On December 31, 2024

    5 Feb 2025, 12:24PM Unaudited financial results for the quarter / nine months ended on December 31, 2024
  • Zydus Lifesciences - Press Release

    30 Jan 2025, 2:19PM Zydus Lifesciences Limited has informed the Exchange regarding a press release dated January 30, 2025, titled ""Celebrating the Legacy of Excellence a
  • Zydus Lifesciences - Announcement under Regulation 30 (LODR)-Press Release / Media Release

    30 Jan 2025, 2:21PM Celebrating the Legacy of Excellence and Innovation Zydus Takeda Healthcare marks 25 years of manufacturing operations in India.
  • Zydus Lifesciences - Copy of Newspaper Publication

    29 Jan 2025, 3:12PM Zydus Lifesciences Limited has informed the Exchange about Copy of Newspaper Publication
  • Zydus Lifesciences

    28 Apr 2025 , 11:17AM Zydus Lifesciences: USFDA issues six observations after Gujarat API unit inspection; none related to data integrity
  • Zydus Lifesciences

    21 Apr 2025 , 10:01AM Zydus Medtech and Braile Biomedica signed a global licence deal to commercialise Transcatheter Aortic Valve Implantation (TAVI) technology in India, Europe and other select markets. This agreement marks a significant step in Zydus MedTech’s strategic expansion into the fastgrowing interventional cardiology segment. The global TAVI market is currently valued at over $6 billion.
  • Zydus Lifesciences

    15 Apr 2025 , 8:55AM The company will acquire 85.6% equity shares of Amplitude Surgical SA, France, at a price of Euro 6.25 per equity share, aggregating to a consideration value of Euro 256.8 million. It also received a final nod from the USFDA for Jaythari (Deflazacort) Tablets, a muscular dystrophy treatment drug. Positive
  • Zydus Lifesciences

    19 Mar 2025 , 8:57AM The company received final approval from the United States Food and Drug Administration (USFDA) to manufacture Apalutamide tablets in a 60 mg strength. Apalutamide is an androgen receptor inhibitor used for the treatment of patients with metastatic castration-sensitive prostate cancer. Apalutamide tablets had annual sales of $1,099.8 million in the United States, according to IQVIA MAT January 2025. Positive
  • Zydus Lifesciences

    17 Mar 2025 , 10:23AM The company has received final approval from the U.S. Food and Drug Administration (USFDA) to manufacture and market Eluxadoline Tablets (75 mg and 100 mg), a key treatment for irritable bowel syndrome with diarrhea (IBS-D) in adults. This milestone strengthens Zydus’ position in the U.S. generics market and is expected to boost its revenue stream.
  • Zydus receives final nod from USFDA for Methenamine Hippurate Tablets

    12 Mar 2025 , 1:37PM Methenamine Hippurate tablets are used for suppressive treatment of UTI
  • Zydus Life to acquire controlling 85.6% stake of amplitude surgical SA.

    11 Mar 2025 , 1:51PM Zydus Life to acquire controlling 85.6% stake of amplitude surgical SA, France for Rs. 2,442 cr.
  • Zydus Life gets final US FDA nod for Ketoconazole Shampoo

    10 Mar 2025 , 10:41AM Ketoconazole is an antifungal medication used to treat dandruff, fungal infections
  • Zydus Lifesciences

    6 Mar 2025 , 9:45AM The firm received the final approval from the United States Food and Drug Administration to manufacture Dasatinib Tablets. Positive
  • Zydus Life will develop combination vaccine to offer protection against shigellosis, typhoid

    4 Mar 2025 , 11:17AM TCV-Shigella combination vaccine aims to protect children below 5 years against shigellosis and typhoid
  • Zydus Lifesciences

    27 Feb 2025 , 11:44AM Company becomes first in India to launch protection against new strain of influenza virus.
  • Zydus Lifesciences

    24 Feb 2025 , 12:26PM Zydus received final approval from USFDA for Ibuprofen and Famotidine Tablets, 800 mg/26.6 mg.
  • Zydus Lifesciences

    17 Feb 2025 , 8:56AM The United States Food and Drug Administration closed its inspection at company's API manufacturing plant at Ambernath, Maharashtra with zero observations. Positive
  • Zydus Lifesciences

    13 Feb 2025 , 9:49AM Zydus Lifesciences Ltd. on Wednesday said it has signed an exclusive development, licensing, supply and commercialisation pact with Synthon BV of the Netherlands for a novel oncology product for an undisclosed target. The novel 505(B)(2) oncology product is likely to be filed in 2026 and will offer additional strengths that are intended to provide reduced pill burden, flexibility for dose adjustment and enhanced patient compliance.
  • Zydus Lifesciences

    23 Jan 2025 , 9:35AM The pharmaceutical company has received US FDA orphan drug designation for Usnoflast which is used for the treatment of amyotrophic lateral sclerosis.
  • Zydus Lifesciences

    20 Jan 2025 , 9:34AM Zydus Life: Company has received approval from USFDA to conduct clinical trial for ‘Usnoflast’, an inflammation drug. Positive
  • Zydus Lifescience

    7 Jan 2025 , 11:31AM US FDA Accepts For Filing and Grants Priority Review to Zydus Life’s US-based Arm & Fortress Bio’s NDA for CUTX-101.
  • Zydus Lifesciences

    27 Nov 2024 , 11:14AM Zydus Lifesciences: Company is eyeing M&A, licensing to build its US Specialty Business. Positive
  • Stock Update: Zydus Lifesciences Limited Q2FY2025 Results Review

    19 Nov 2024 , 11:16AM Stock Update: Zydus Lifesciences Limited Q2FY2025 Results Review: Soft Q2: Topline guidance lowered
  • Zydus Life gets in principle nod from WHO for Typhoid Injection, ZyVac

    23 Oct 2024 , 11:53AM WHO prequalifies Zydus's Typhoid Vi Conjugate Vaccine, ZyVac TCV.
  • Zydus Lifesciences

    18 Oct 2024 , 11:11AM Zydus Lifesciences gets US FDA final approval for Fludrocortisone Acetate tablets USP, 0.1 mg. Fludrocortisone acetate tablets are indicated as partial replacement therapy for primary and secondary adrenocortical insufficiency in Addison's disease
  • Stock Update: Zydus Lifesciences

    4 Oct 2024 , 12:50PM Stock Update: Zydus Lifesciences Ltd – R&D advancements to drive growth
  • Zydus Lifesciences

    3 Oct 2024 , 1:33PM Company gets USFDA nod to produce prostate cancer drug also US FDA classifies Pharmez Unit In Ahmedabad as voluntary action indicated
  • Zydus Lifesciences

    18 Sep 2024 , 11:04AM Zydus Lifesciences board approves business transfer agreement to purchase API business of Sterling Biotech for ₹84 crores
  • Zydus Lifesciences

    16 Sep 2024 , 12:23PM Company's Arm Zydus Lifesciences Global FZE signs exclusive licensing & supply agreement with US-based Viwit Pharmaceuticals for Gadobutrol Injection & Gadoterate Meglumine Injection for the US market. (Positive)
  • Zydus Lifesciences gets USFDA nod for Parkinson's drug

    28 Aug 2024 , 10:48AM Zydus gets final nod from USFDA for Amantadine extended-release capsules 68.5 mg and tentative approval for 137 mg
  • Zydus Lifesciences

    27 Aug 2024 , 10:07AM The company clarified that an approval for the generic product in the name of gAsacol HD (Mesalamine 800 mg) of the Company, marketed in the United States of America, has been given by the USFDA to another company. This could lead to a potential competition and impact the sales and profits from the said product and the same is on anticipated lines. The impact of the same is already factored by the Company in its sales and operating profit (EBITDA) expectations for FY2025 shared in the post results investors call on August 9, 2024. The Company had guided for an improvement in consolidated EBITDA margin by about 150 basis points in FY25E as compared to 27.5% ENITDA margin in FY24 and has also guided for high terms growth. (Positive)
  • Stock Update: Zydus LifeScience

    13 Aug 2024 , 11:55AM Stock Update: Zydus Life Science – Good Q1, Healthy Outlooked maintained
  • Zydus Life Science

    13 Aug 2024 , 10:54AM MSCI has done seven addition and one deletion from India MSCI Emerging Market Index. Zydus Life to be included in MSCI August review. Positive
  • Zydus LifeScience

    22 Jul 2024 , 10:13AM Zydus receives approval from COFEPRIS of Mexico to market  Bhava™ (Bevacizumab biosimilar) to treat various cancers. The Mexican regulatory authority COFEPRIS (Federal Commission for the Protection Against Sanitary Risk), has granted marketing approval for BhavaTM, a Bevacizumab biosimilar. BhavaTM (Bevacizumab), will be marketed in different strengths of 100 mg/4 ml and 400 mg/16 ml and used in the treatment of metastatic Colorectal Cancer (mCRC), non-squamous non-small cell lung cancer, metastatic breast cancer, glioblastoma, advanced and/or metastatic renal cell carcinoma and ovarian cancer patients. (Positive)
  • Zydus Lifesciences

    19 Jul 2024 , 1:43PM Zydus has received final approval for its New Drug Application (NDA) from the USFDA to market ZituvimetTM XR (sitagliptin and metformin hydrochloride) extended-release tablets. With this, Zydus has all three NDAs of Sitagliptin (base) and combination franchise approved through the 505(b)(2) route. Notably, all the three NDAs achieved First-Cycle Approval (FCA). ZituvimetTM XR (sitagliptin and metformin hydrochloride) extended-release tablets are indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus. (Positive)
  • Zydus receives final approval from USFDA for its NDA Zituvimet

    19 Jul 2024 , 12:01PM Indicate as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus
  • Zydus Life science

    19 Jul 2024 , 10:39AM The Company has received a report from the United States Food and Drug Administration (“USFDA”) for the inspection conducted at its injectables manufacturing facility located at Jarod, near Vadodara, Gujarat, India between April 15 and April 23, 2024. The USFDA has determined that the inspection classification of this facility is “Official Action Indicated” (OAI). (Negative)
  • Zydus Lifescience

    18 Jul 2024 , 1:06PM Zydus announces non-exclusive patent licensing agreement with Takeda for ‘Vault® ’ (Vonoprazan) in India. Zydus Lifesciences Limited (including its subsidiaries/affiliates hereafter referred to as “Zydus”) a discovery-driven global lifesciences company has entered into a non-exclusive patent licensing agreement with Takeda Pharmaceutical Company to market the novel Potassium Competitive Acid Blocker (P-CAB) Vonoprazan in India. The drug will be marketed under the brand name of Vault® in India. (Positive)
  • Zydus Life Science

    11 Jul 2024 , 10:46AM Zydus Lifesciences has received final approval from the United States Food and Drug Administration (USFDA) to market Sacubitril and Valsartan Tablets, 24 mg/26 mg, 49 mg/51 mg, and 97 mg/103 mg (USRLD: Entresto tablets). Sacubitril and Valsartan combination is used to treat chronic heart failure in adults to help reduce the risk of death and hospitalization. The drug will be manufactured at the group’s formulation manufacturing facility in Moraiya, Ahmedabad (India). Sacubitril and Valsartan tablets had annual sales of USD 5,483 mn in the United States (IQVIA MAT May 2024). (Positive)
  • Zydus Life gets tentative approval from USFDA for Azilsartan Medoxomil tablets

    4 Jul 2024 , 2:46PM Azilsartan Medoxomil tablets are used to treat high blood pressure
  • Zydus Lifesciences

    18 Jun 2024 , 11:27AM Zydus Lifesciences Limited (including its subsidiaries/ affiliates, hereafter referred to as “Zydus”) has received tentative approval from the United States Food and Drug Administration (USFDA) to market Azilsartan Medoxomil and Chlorthalidone Tablets, 40 mg/12.5 mg and 40 mg/25 mg (USRLD: Edarbyclor tablets). Azilsartan and chlorthalidone is an angiotensin II receptor blocker (ARB) and a thiazide like diuretic combination product indicated for the treatment of high blood pressure (hypertension), to lower blood pressure. The drug will be manufactured at the group’s formulation manufacturing facility in Ahmedabad SEZ - II, India. Azilsartan Medoxomil and Chlorthalidone Tablets had annual sales of USD 77.9 mn in the United States (IQVIA MAT March 24). (Positive)
  • Zydus Life gets tentative USFDA nod to market Azilsartan Medoxomil & Chlorthalidone Tablets

    14 Jun 2024 , 1:14PM Azilsartan & Chlorthalidone is used for the treatment of high blood pressure
  • Zydus Life gets final US FDA approval for theophylline extended-release tablets

    22 May 2024 , 12:32PM Theophylline is used to treat asthma and chronic obstructive pulmonary disease
  • Zydus Life signs exclusive licensing & supply agreement with MSN

    17 May 2024 , 10:24AM Cabozantinib tablets are used alone to treat Advanced Kidney Cancer
  • Zydus Life Science

    13 May 2024 , 9:55AM Zydus Lifesciences has received final approval from the United States Food and Drug Administration (USFDA) to market Dexamethasone Tablets USP, 1 mg. Dexamethasone is used to treat conditions such as arthritis, blood/hormone disorders, allergic reactions, skin diseases, eye problems, breathing problems, bowel disorders, cancer and immune system disorders. The product will be manufactured at the group’s formulation manufacturing facility at Baddi, Himachal Pradesh. Dexamethasone Tablets USP, 1 mg had annual sales of USD 1.8 mn in the United States (IQVIA MAT March 24). (Positive)
  • Zydus receives final approval from USFDA for Dapsone Gel, 7.5%

    9 May 2024 , 12:20PM Zydus Life receives USFDA Approval for Dapsone Gel, which is used to treat acne
  • Zydus Lifesciences

    26 Apr 2024 , 2:34PM Zydus receives final approval from USFDA for Tretinoin Cream USP, 0.1%. Tretinoin cream is used to treat acne. The drug will be manufactured at the group’s topical manufacturing facility at Changodar, Ahmedabad (India). Tretinoin Cream USP, 0.1% had annual sales of USD 54.8 mn in the United States (IQVIA MAT Feb-24). (Positive)
  • Zydus Lifesciences

    24 Apr 2024 , 10:50AM The USFDA conducted an inspection at the Injectable Manufacturing site situated at Jarod, near Vadodara. The inspection was conducted from April 15 to April 23, 2024. The inspection closed with 10 observations. The Company will closely work with the USFDA to address and respond to the observations in an expeditious manner. Negative
  • Lupin, Zydus Lifesciences

    24 Apr 2024 , 10:49AM As per the media sources there is a setback for Lupin and Zydus as their Launch of Mirabegron Extended-Release Tablets, 25 mg, in the United States, after having received an approval from the USFDA has been cancelled. Launch of generic Myrbetriq has been blocked until any further orders by the court as the US Court of Appeals for the Federal Circuit.
  • Zydus Life launches Mirabegron extended-release tablets in the US

    22 Apr 2024 , 10:28AM Mirabegron is indicated for the treatment of an Overactive Bladder (OAB)
  • Zydus Lifesciences

    22 Apr 2024 , 9:05AM The company received USFDA nod to launch Miranegron - extended release tablet in the US market. (Positive).
  • Zydus Lifesciences

    2 Apr 2024 , 10:22AM Zydus Lifesciences receives approval for the name ‘Usnoflast’ as recommended name for ZYIL1 from the WHO International Non-proprietary Names (INN). Usnoflast (ZYIL1) is a novel oral small molecule NLRP3 inhibitor discovered at Zydus Research Centre, the R&D arm of Zydus Lifesciences Ltd. Usnoflast is under clinical development in 4 indications : Cryopyrin-Associated Periodic Syndromes (CAPS), Amyotrophic Lateral Sclerosis (ALS), Parkinson’s disease and Ulcerative Colitis. Positive.
  • Stock Update: Zydus Life Science

    21 Mar 2024 , 11:43AM Stock Update: Zydus Life Science - Specialty portfolio growth to drive margins.
  • Zydus life Science

    18 Mar 2024 , 9:56AM Zydus receives final approval from USFDA and 180 days CGT exclusivity for Finasteride and Tadalafil Cap Capsules. Zydus is the first approved applicant for Finasteride and Tadalafil Capsules, 5 mg/5 mg, as defined in section 505(j)(5)(B)(v)(III) of the FD&C Act and therefore is eligible for 180 days of CGT exclusivity. Finasteride and Tadalafil is used to treat benign prostatic hyperplasia. The drug will be manufactured at the group’s formulation manufacturing facility at Ahmedabad SEZ II, India. Positive.
  • Zydus Life sciences

    14 Mar 2024 , 10:52AM Company introduces IBYRA a generic version of Olaparib for cancer patients in India. This will be treated for breast cancer, Ovarian cancer and Pancreatic cancer. (Positive)
  • Zydus Lifesciences

    11 Mar 2024 , 12:05PM The company has received the EIR report from the USFDA for the inspection conducted at the API Ahmedabad facility. The company had earlier received Post Application Action Letter from the USFDA for the same inspection confirming that the inspected facility has been considered as ready to commercially manufacture and supply the API. This facility underwent an inspection from 14th to 22nd Dec 2023 and has been classified as Voluntary Action Indicated (VAI). (Positive)
  • Zydus Life Science

    7 Mar 2024 , 12:36PM The company has received Post Application Action Letter from the USFDA for the inspection conducted at the Ahmedabad API facility of Zydus Lifesciences Limited, confirming that the inspected facility has been considered as ready to commercially manufacture and supply the API. This facility underwent for-cause cGMP surveillance and Pre-Approval Inspection for manufacturing of drug substances Enzylutamide from 14th to 22nd Dec 2023. Positive
  • Zydus Life Science

    26 Feb 2024 , 12:01PM Zydus receives WHO prequalification for Miltefosine formulation and API, A significant milestone for the treatment of Leishmaniasis or Kala Azhar. Leishmaniasis is caused by protozoan parasites which are transmitted by the bite of infected female phlebotomine sandflies. The disease affects some of the world’s poorest people and is associated with malnutrition, population displacement, poor housing, a weak immune system and lack of financial resource. (Positive)
  • Zydus receives WHO prequalification from Miltefosine formulation and API

    26 Feb 2024 , 9:51AM A significant milestone for the treatment of Leishmaniasis or Kala Azhar
  • Zydus Lifesciences

    16 Feb 2024 , 2:39PM Zydus receives Final Approval from the USFDA for Isosorbide Mononitrate Extended-Release, Tablets USP, 30 mg, 60 mg, and 120 mg. Isosorbide mononitrate is used to prevent chest pain (angina) in patients with a certain heart condition (coronary artery disease). The product will be manufactured at the group’s formulation manufacturing facility at Ahmedabad SEZ, India. Isosorbide Mononitrate Extended-Release, Tablets USP, 30 mg, 60 mg, and 120 mg had annual sales of USD 47 mn in the United States (IQVIA Dec. Nov. 2023). (Positive)
  • Stock Update: Zydus Life Science

    14 Feb 2024 , 11:33AM Zydus Life Science Ltd. - Good Q3, Margin guidance revised upwards.
  • Zydus Life Science

    8 Feb 2024 , 3:05PM Zydus receives Final Approvals from the USFDA for Dexamethasone Tablets USP, 0.5 mg, 0.75 mg, 1.5 mg, 4 mg and 6 mg and Dexamethasone Tablets USP, 2 mg. Dexamethasone is used to treat a number of different conditions, such as inflammation, severe allergies, adrenal problems, arthritis, asthma, blood or bone marrow problems, kidney problems, skin conditions, and flare-ups of multiple sclerosis. The products will be manufactured at the group’s formulation manufacturing facility at Baddi, Himachal Pradesh. Dexamethasone Tablets USP, 0.5 mg, 0.75 mg, 1.5 mg, 4 mg and 6 mg had annual sales of USD 22 mn and Dexamethasone Tablets USP, 2 mg has annual sales of USD 6 mn in the United States (IQVIA Dec. Nov. 2023). (Positive)
  • Zydus Lifesciences

    6 Feb 2024 , 10:29AM Zydus Lifesciences Board at its aforesaid meeting, will consider a proposal for buyback of fully paid-up equity shares of the Company and the matters necessary and incidental thereto, in accordance with the applicable provisions under the Companies Act, 2013 (including the rules and regulations framed thereunder), the Securities and Exchange Board of India (Buy-back of Securities) Regulations, 2018, as amended, and other applicable laws. Positive
  • Zydus gets final USFDA nod for Gabapentin Tablets

    25 Jan 2024 , 3:22PM Gabapentin is used for the management of Postherpetic Neuraligia (PHN)
  • Zydus Lifesciences subsidiary signs licensing agreement with Synthon BV

    19 Jan 2024 , 10:56AM Zydus, Synthon enter into an exclusive licensing and supply agreement for Palbociclib Tablets for the US market
  • Zydus Lifesciences

    18 Jan 2024 , 10:59AM Zydus receives Final Approvals from the USFDA for Pimavanserin Capsules, 34 mg and Pimavanserin Tablets,10 mg. Pimavanserin is an atypical antipsychotic indicated for the treatment of hallucinations and delusions associated with Parkinson disease psychosis. Both the tablets and the capsules will be manufactured at the group’s formulation manufacturing facility at Ahmedabad SEZ, India. Pimavanserin Capsules, 34 mg had annual sales of USD 149 mn and Pimavanserin Tablets, 10 mg had annual sales of USD 10 mn in the United States (IQVIA Dec. Nov. 2023). (Positive)
  • Zydus Lifesciences

    3 Jan 2024 , 11:02AM CRISIL Ratings has upgraded its rating on the long-term bank facilities and debt programme of Zydus Lifesciences Ltd to ‘CRISIL AAA/Stable’ from 'CRISIL AA+/Positive’ and reaffirmed its 'CRISIL A1+' rating on the short-term bank facilities and commercial paper programme. The rating upgrade reflects CRISIL Ratings expectations of improvement in Zydus Life’s business risk profile on the back of healthy revenue growth of 10-12% annually led by new product launches across markets and ramp up in sales of new chemical entities and biosimilars, while sustaining strong operating margin at 22-24% (Positive)
  • Zydus Lifesciences

    27 Dec 2023 , 10:10AM Zydus Healthcare Limited, a wholly owned subsidiary of the Company has received an intimation under section 143(1) of the Income Tax Act, 1961, determining demand of Rs. 284.58 crores, while processing the Return of Income of ZHL. Based on the assessment and advice of the learned counsel, ZHL does not expect the said intimation to have any material financial impact as abovementioned adjustments are not sustainable in law and are wholly defendable on the facts of the case. (Negative)
  • Stock Update: Zydus Life Science

    26 Dec 2023 , 11:17AM Stock Update: Zydus Life Science- Growth in specialty portfolio to lift margins.
  • Zydus Life Science

    18 Dec 2023 , 9:58AM Zydus receives final approval from the USFDA for Lacosamide Tablets. Lacosamide is indicated to treat partial-onset seizures. It is also used with other medicines to treat primary generalized tonic-clonic seizures. The product will be manufactured at the group’s formulation manufacturing facility in Moraiya, Ahmedabad. Lacosamide Tablets USP, 50 mg, 100 mg, 150 mg, and 200 mg had annual sales of USD 249 mn in the United States (IQVIA Dec. Oct. 2023). (Positive)
  • Zydus Life Science

    15 Dec 2023 , 11:34AM Zydus receives final approval from the USFDA for Cyclophosphamide Capsules USP, 25 mg and 50 mg. Cyclophosphamide is a chemotherapy medication that slows the growth of cancer cells. It treats lymphoma, myeloma, leukemia, breast cancer and ovarian cancer. The drug will be manufactured at the group’s formulation manufacturing facility at Ahmedabad SEZ. Cyclophosphamide Capsules USP, 25 mg and 50 mg had annual sales of USD 6 mn in the United States (IQVIA MAT October,2023). (Positive)
  • Zydus Life gets final nod from USFDA for Darunavir tablets 600 & 800 mg

    15 Dec 2023 , 10:50AM Gets tentative nod for 75 mg & 150 mg Darunavir tablets
  • Zydus Life gets Final USFDA approval for Cyclophosphamide Capsules USP

    14 Dec 2023 , 2:26PM Cyclophosphamide is a chemotherapy medication that slows the growth of cancer cells
  • Zydus Life inks licensing pact with Daewoong Pharma for Leuprolide in US

    11 Dec 2023 , 10:32AM Zydus, Daewoong Pharma announce licensing agreement for development and commercialization of Leuprolide Long-Acting Injectable in the US
  • Zydus Lifesciences

    6 Dec 2023 , 3:09PM Zydus receives Final Approval from the USFDA for Methylene Blue Injection. It is the generic version of the Reference Listed Drug (RLD) ProvayBlue® Injection. Methylene Blue Injection is an oxidation-reduction agent indicated for the treatment of pediatric and adult patients with acquired methemoglobinemia. Methylene Blue Injection, 10mg/2ml and 50mg/5ml had an annual sale of approximately USD 73.4 mn in the United States (IQVIA MAT Oct-2023). (Positive)
  • Zydus receives final nod from USFDA for Methylene Blue Injection

    6 Dec 2023 , 2:53PM Methylene Blue Injection, a drug use to treat a condition called methemoglobinemia
  • Zydus receives final approval from the USFDA for Ivabradine Tablets

    1 Dec 2023 , 12:42PM Ivabradine is indicated to reduce the risk of hospitalization for worsening heart failure in adult patients with stable
  • Zydus Lifesciences

    1 Dec 2023 , 12:24PM Zydus receives final approval from the USFDA for Ivabradine Tablets, 5 mg and 7.5 mg. Ivabradine is indicated to reduce the risk of hospitalization for worsening heart failure in adult patients with stable, symptomatic chronic heart failure with reduced left ventricular ejection fraction. Zydus was one of the first ANDA applicants to submit a substantially complete ANDA with a paragraph IV certification for Ivabradine Tablets, 5 mg and 7.5 mg and therefore may be eligible for 180 days of shared generic exclusivity for Ivabradine Tablets, 5 mg and 7.5 mg. Ivabradine Tablets, 5 mg and 7.5 mg had annual sales of USD 136.5 mn in the United States (IQVIA MAT October,2023). (Positive)
  • Stock Update: Zydus Life Science

    8 Nov 2023 , 11:38AM Stock Update: Zydus Life Science – Result update - Mixed Q2; Outlook robust
  • Zydus Life Q2FY24 results – Mixed bag earnings

    7 Nov 2023 , 2:06PM Zydus Life Q2FY24 results – Mixed bag earnings - Sales miss; margins expand on cost rationalization
  • Zydus, Guardant Health to jointly promote the Guardant360

    2 Nov 2023 , 10:21AM The agreement demonstrates a shared commitment to advance precision medicine and improve patient outcomes in the region
  • Zydus Life to acquire LiqMeds Group for Rs. 689 cr

    31 Oct 2023 , 2:43PM Board of Directors of Zydus Lifesciences approves entering into the Sale and Purchase Agreement (SPA) amongst the Sellers
  • Zydus Lifesciences

    25 Oct 2023 , 10:45AM Zydus Lifescience initiates Phase II clinical trial of ZYIL1, a novel oral NLRP3 inflammasome inhibitor in patients with Amyotrophic Lateral Sclerosis (ALS). The Phase 2 clinical trial will assess the safety and efficacy of ZYIL1 in Amyotrophic Lateral Sclerosis (ALS) patients. ALS is a rare, progressive and fatal neurodegenerative disease, with an average life expectancy of 3 to 5 years from the time of symptom onset. ALS affects approximately 31,000 people in the U.S.A and on average 5,000 new patients are diagnosed every year with this disease in USA as per statistics from Centers for Disease Control and Prevention (CDC). More than 30,000 people are estimated to be living with ALS in Europe (European Union and United Kingdom), while India has an estimated 75,000 people living with ALS. (Positive)
  • Zydus Lifesciences initiates Phase II clinical trial of ZYIL1

    25 Oct 2023 , 9:55AM Zydus Life initiates phase-II clinical trial of ZYIL1, a novel oral inflammasome inhibitor
  • Zydus Lifesciences

    23 Oct 2023 , 12:09PM : Zydus receives USFDA approval for ZITUVIOTM to treat adult patients with type 2 diabetes mellitus. ZITUVIOTM contains active ingredient Sitagliptin, a dipeptidyl peptidase-4 (DPP-4) inhibitor indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus. According to IQVIA™ (MAT Aug-2023), U.S. market for DPP-IV inhibitors and its combinations is US$ 10 bn. View – As there are many players in the Sitagliptin molecule, this news will have neutral impact on the stock.
  • Zydus Lifesciences

    9 Oct 2023 , 11:45AM Zydus receives final approval from the USFDA for Sugammadex Injection, 200 mg/2 mL (100 mg/mL) and 500 mg/5 mL (100 mg/mL), Single-Dose Vial. Sugammadex Injection is indicated for the reversal of neuromuscular blockade induced by rocuronium bromide and vecuronium bromide in adults undergoing surgery. Sugammadex Injection, 200 mg/2 mL (100 mg/mL) and 500 mg/5 mL (100 mg/mL), Single[1]Dose Vial had annual sales of USD 986 mn in the United States (IQVIA MAT Aug 2023).
  • Zydus announces IND clearance of a novel Anti-PCSK9 candidate

    29 Sep 2023 , 3:30PM Zydus Lifesciences gets CDSCO clearance to initiate the Phase I clinical study of its Novel PCSK9 inhibitor
  • Zydus Lifesciences

    29 Sep 2023 , 3:12PM Zydus announces IND clearance of a novel Anti-PCSK9 candidate. It has received permission from CDSCO India, to initiate the Phase I clinical study of its novel PCSK9 inhibitor. The Phase I prospective randomised, double-blind, placebo-controlled study which will study the safety and tolerability of anti-PCSK9 product administered subcutaneously in healthy human volunteers.
  • Zydus Lifesciences

    21 Sep 2023 , 9:41AM The company has received final approval from the United States Food and Drug Administration (USFDA) for Clindamycin Phosphate Gel USP, 1%. Clindamycin Phosphate Gel USP, 1% is used to treat acne and had annual sales of USD 37 mn in the United States (IQVIA MAT July 2023). Positive for the stock.
  • Zydus Lifesciences

    20 Sep 2023 , 10:14AM The company has received the EIR report from the USFDA for the inspection conducted at the formulation manufacturing facility named ‘SEZ 2’ located at Pharmez, Ahmedabad from 3rd to 7th July, 2023. This was a Pre-Approval Inspection (PAI) and had concluded with NIL observations. Positive for the stock.
  • Zydus gets final USFDA approval for Isotretinoin Capsules used for treatment for severe acne

    31 Aug 2023 , 1:59PM Isotretinoin Capsules is used to treat severe cystic acne that has not responded to other treatmen
  • Zydus gets final nod from USFDA for Zinc Sulfate Injection

    24 Aug 2023 , 12:01PM Zydus Life gets USFDA nod for Zinc Sulfate Injection used in paediatric patients as a source of zinc for parenteral nutrition
  • Zydus Lifesciences

    18 Aug 2023 , 10:29AM The company has received final approval from the USFDA for Doxepin tablets used to treat insomnia. Doxepin tablets, 3 mg and 6 mg had annual sales of $43.4 million in the U.S. Positive for the stock
  • Zydus Lifesciences

    3 Aug 2023 , 10:41AM Zydus Lifesciences has received final approval from the USFDA to manufacture and market Indomethacin suppositories, 50 mg. Zydus Indomethacin suppositories 50 mg is the generic of RLD Indocin suppositories, 50 mg. The company gains 180 days CGT exclusivity to market this product. Indomethacin suppositories is a non-steroidal, anti-inflammatory drug indicated for moderate to severe rheumatoid arthritis including acute flares of chronic disease, moderate to severe ankylosing spondylitis, moderate to severe osteoarthritis, acute painful shoulder (bursitis and/or tendinitis) and acute gouty arthritis. Indomethacin suppositories 50mg had an annual sale of approximately USD 95 mn in the United States (IQVIA MAT April-2023). Strongly positive for Zydus Life
  • Zydus Lifesciences

    27 Jul 2023 , 1:38PM Zydus Lifesciences Ltd. has received final approval from the USFDA for Plerixafor Injection 24 mg/1.3 mL (20 mg/mL), Single Dose Vial (USRLD: Mozobil injection, 24 mg/1.2 mL (20 mg/mL) It is used by patients with certain types of cancer lymphoma – NHL multiple myeloma – MM to prepare them for stem cell transplant. The drug will be manufactured at Zydus Life’s SEZ, Ahmedabad facility. Plerixafor Injection, 24 mg/1.2 mL (20 mg/mL), Single-Dose Vial had annual sales of USD 210 mn in the United States (IQVIA MAT May 2023). Positive for the stock.
  • Zydus Lifesciences

    10 Jul 2023 , 10:38AM Zydus Lifesciences’ manufacturing facility at SEZ – 2 located at Pharmez, Ahmedabad, which underwent a USFDA inspection from July 2 to July 7 2023 for a pre-approval inspection, closed without any observations. Positive.
  • Zydus Lifesciences

    4 Jul 2023 , 2:03PM Zydus Lifesciences Ltd. received final approval from the USFDA for Oxcarbazepine tablets USP 150, 300, and 600 mg (US RLD: Trileptal) which is used to treat seizures (epilepsy) and will be manufactured at its Baddi facility at Himachal Pradesh. The drug has annual market size of USD 105 million as of May 23, as per IQVIA. The product is already being manufactured by players like Sun Pharma and Glenmark Pharma and 4 other manufacturers. Hence, it’s a marginally positive development for the stock.
  • Zydus gets final nod from the USFDA for Oxcarbazepine Tablets

    4 Jul 2023 , 11:52AM Oxcarbazepine Tablets that are used alone or with other medications to treat seizure
  • Zydus Lifesciences

    3 Jul 2023 , 12:03PM Zydus Life has received EIR from the USFDA for the inspection conducted at its manufacturing facility located at Pharmrez, Ahmedabad. The inspection has been classified as Voluntary Action Indicated (VAI). Positive read through for the stock.
  • Zydus Lifesciences

    3 Jul 2023 , 12:01PM Zydus Life has received EIR from the USFDA for the inspection conducted at its manufacturing facility located at Pharmrez, Ahmedabad. The inspection has been classified as Voluntary Action Indicated (VAI). Positive read through for the stock.
  • Stock Update: Zydus Lifesciences

    3 Jul 2023 , 11:15AM Stock Update: Zydus Lifesciences (Company Update): Product approvals, market share gains to boost growth
  • Zydus Lifesciences

    26 Jun 2023 , 11:31AM Zydus Lifesciences Ltd.’s subsidiary Zydus Animal Health and Investments Ltd. has agreed to acquire 6.5% stake or 65.07 lakh shares in Mylab Discovery Solutions Pvt Ltd. for Rs. 106 Cr. Mylab is in the business of researching, developing, and selling in-vitro diagnostic kits, equipment and re-agents and related therapeutic products that are linked to offering diagnostic portfolio of products to Hospitals and labs. The deal is likely to have taken place at an expensive level of ~17x Mylabs’ FY23 revenue of Rs. 95 Cr. However, the number of shares that Zydus will hold in Mylab will depend on the performance of Mylab in FY24. Neutral to marginally negative for the stock.
  • Zydus Life

    14 Jun 2023 , 10:27AM Zydus Life’s injectables manufacturing facility at Zydus Biotech Park in Changodar, Ahmedabad, underwent USFDA inspection from June 5, 2023, to June 13, 2023. The cGMP inspection concluded with NIL observations. Positive for the stock. The company has complex injectable filings done and plans to launch 1-2 important products in FY24. The company expects the shortages faced in the US will help it give good momentum. As of now, injectables (oncology) is likely to become a sizable business only after FY25. The company has 2 injectable plants including Changodar and Jarod in India.
  • Zydus Lifesciences

    13 Jun 2023 , 3:17PM Zydus Lifesciences has received final approval from the United States Food and Drug Administration (USFDA) to manufacture and market Diclofenac Sodium and Misoprostol Delayed Release Tablets USP, 50mg/200 mcg and 75mg/200 mcg (USRLD: Arthrotec Delayed-Release Tablets). Diclofenac Sodium and Misoprostol Delayed Release Tablets USP, 50mg/200 mcg and 75mg/200 mcg had annual sales of USD 13 mn in the United States (IQVIA MAT Mar. 2023). Positive read through for the stock.
  • Zydus Life gets final USFDA nod for Varenicline tablets

    13 Jun 2023 , 3:06PM Varenicline tablets is use to treat smoking addiction
  • Zydus Lifesciences

    13 Jun 2023 , 2:57PM Zydus Lifesciences has received final approval from the United States Food and Drug Administration (USFDA) to manufacture and market Varenicline Tablets, 0.5 mg, and 1 mg (USRLD: Chantix Tablets). The product will be launched shortly. Varenicline tablets is indicated to treat smoking addiction. The drug will be manufactured at the group’s formulation manufacturing facility at Ahmedabad SEZ, India. Varenicline Tablets, 0.5 mg and 1 mg had annual sales of USD 501 mn in the United States (IQVIA MAT Mar. 2023). Positive read through for the stock.
  • Zydus Life sciences

    12 Jun 2023 , 10:09AM Zydus Lifesciences Limited has received final approval from the United States Food and Drug Administration (USFDA) for Balsalazide Disodium Capsules USP, 750 mg (USRLD: Colazal Capsules, 750mg). Balsalazide Disodium is used to treat bowel diseases like ulcerative colitis. The product will be manufactured at the group’s formulation manufacturing facility in SEZ, Ahmedabad (India).Balsalazide Disodium Capsules USP, 750 mg had annual sales of USD 29 mn in the United States (IQVIA MAT April 2023). Positive read through for the stock.
  • Zydus Lifesciences

    9 Jun 2023 , 11:18AM Zydus Lifesciences announced the commencement of Phase of IV Real World Data registry trial “EVIDENCES – XI” for Saroglitazar Magnesium in NAFLD patients with co-morbidities such as type 2 diabetes mellitus, dyslipidaemia, or metabolic syndrome.
  • Zydus Lifesciences

    8 Jun 2023 , 5:06PM Zydus Lifesciences Ltd. has received final approval from the USFDA for Esomeprazole Magnesium for delayed release oral suspension, 20 and 40 mg, (USRLD: Nexium Delayed Release for Oral Suspension, 20 and 40 mg) It is used to treat certain stomach and esophagus problems such as acid reflux and ulcer. Esomeprazole Magnesium for Delayed-Release Oral Suspension, 20 mg and 40 mg had annual sales of USD 42 mn in the US (IQVIA MAT April 2023). Positive read through for the stock.
  • Zydus gets USFDA Nod for Esomeprazole Magnesium oral suspension

    8 Jun 2023 , 1:51PM Esomeprazole is used to treat certain stomach and esophagus problems
  • Zydus Lifesciences

    5 Jun 2023 , 10:13AM The U.S. FDA inspection of the company’s animal health drug manufacturing facility at SEZ, Ahmedabad was closed with nil observations. Positive. The company has sold its Animal Health business at Rs. 2,921 Cr. for India and certain other countries but has the business continuing for the US, Europe, and other emerging markets. The healthcare business generated revenue of Rs. 513 Cr in FY20, ~4.0% of the consolidated revenue and ~3.0% of the consolidated EBITDA.
  • Zydus Lifesciences

    11 May 2023 , 10:02AM Zydus Life has received Establishment Inspection Report (EIR) for its products’ Pre-Approval Inspection (PAI) at Moraiya. Highly positive.
  • Zydus Lifescience

    5 May 2023 , 9:44AM Zydus Lifesciences receives final approval from the USFDA to manufacture and market Sucralfate Tablets USP 1 gm (USRLD: Cara fate tablets, 1 gm) which is used to treat and prevent ulcers in the intestines by forming a coating over ulcers, protecting the area from further injury. It will be manufactured at SEZ facility at Ahmedabad. The drug has annual sales of USD 84.0 million in the US. Positive.
  • Zydus Lifesciences

    25 Apr 2023 , 3:20PM Zydus Life has received final approval from the USFDA to manufacture and market Metronidazole topical cream 0.75% (USRLD: MetroCream, 0.75%) It is an anti-biotic used on the skin to treat a certain skin disorder known as rosacea, a type of adult acne. It will be manufactured at the company’s facility at Changodar, Ahmedabad. The drug has annual sales of USD 25 million as of Feb 23 as per IQVIA MAT. Positive for the stock.
  • Zydus Life gets final USFDA nod for Metronidazole topical cream

    25 Apr 2023 , 3:08PM Metronidazole is an antibiotic used on the skin to treat a certain skin disorder
  • Zydus Lifesciences

    24 Apr 2023 , 12:49PM Zydus Lifesciences has received final approval from the USFDA for Icosapent Ethyl Capsules 0.5 g and 1 g (USRLD: Vascepa capsules) which are indicated as an adjunct to diet to reduce triglyceride levels in adult patients. It’s a highly positive development for Zydus Life as Vascepa is a blockbuster drug with an annual market size of USD 1.32 billion (as per IQVIA MAT Feb 23) with relatively lower competition. Dr. Reddy’s, Hikma, Apotex and Teva manufacture its generic, from before.
  • Zydus Lifesciences

    24 Apr 2023 , 9:55AM Zydus Lifesciences has received final approval from the USFDA for Icosapent Ethyl Capsules 0.5 g and 1 g (USRLD: Vascepa capsules) which are indicated as an adjunct to diet to reduce triglyceride levels in adult patients. It’s a highly positive development for Zydus Life as Vascepa is a blockbuster drug with an annual market size of USD 1.32 billion (as per IQVIA MAT Feb 23) with relatively lower competition. Dr. Reddy’s, Hikma, Apotex and Teva manufacture its generic, from before.
  • Zydus Lifesciences

    21 Apr 2023 , 10:19AM Zydus Lifesciences has received final approval from the USFDA to manufacture and market Metoprolol Tartrate tablets USP 25, 50 and 100 mg (USRLD: Lopressor) It is used with or without medications to treat high blood pressure (hypertension) The tablets had annual sales of USD 45.2 million in the US as per IQVIA MAT Feb 2023. Positive development for the stock.
  • Zydus receives final approval from the USFDA for Roflumilast Tablets

    19 Apr 2023 , 3:20PM Roflumilast reduces inflammation in the lungs that leads to chronic obstructive pulmonary disease
  • Zydus Lifesciences

    19 Apr 2023 , 10:33AM Zydus Life has received final approval from the USFDA to manufacture and market Estradiol Transdermal system, USP, 0.014 mg/day (weekly) which is an equivalent to Menostar Transdermal system who had annual sales of USD 1.9 million in the US as per IQVIA MAT Feb 23. Positive development.
  • Zydus receives final approval from the USFDA for Estradiol Transdermal System

    19 Apr 2023 , 10:20AM Zydus Lifesciences gets final approval from the US FDA to market Estradiol Transdermal System
  • Zydus Lifesciences

    17 Apr 2023 , 11:44AM Zydus Lifesciences has received final approval from the USFDA to manufacture and market Isoproterenol Hydrochloride Injection USP 0.2 mg/mL and 1 mg/5 mL, single dose vials (US RLD: Isuprel injection) The injection is indicated for treating cardiovascular concerns. The drug will be manufactured at its injectable facility at Jarod, near Vadodara (India). It had market size of USD 28.5 million in the US as per IQVIA MAT Feb 2023. Positive for the stock.
  • Zydus gets final US FDA nod for Tavaborole Topical Solution

    11 Apr 2023 , 3:18PM Tavaborole Topical Solution is used to treat fungal toenail infections
  • Zydus Lifesciences

    11 Apr 2023 , 10:55AM Zydus Lifesciences Ltd. has received final approval from the USFDA to manufacture and market Azithromycin tablets USP 500 mg (US RLD: Zithromax tablets of Pfizer) Azithromycin is to treat bacterial infections such as bronchitis, pneumonia, STDs, infections of the ears, lungs, sinuses, skin, and throat. The drug will be manufactured at the company’s Moraiya facility. The drug has annual sales of USD 20 million, as of Feb 2023, as per IQVIA MAT. Positive for the stock.
  • Zydus Lifesciences

    6 Apr 2023 , 12:50PM Zydus Lifesciences Ltd. has received final approval from the USFDA to manufacture and market Acetazolamide tablets USP 125 and 250 mg (USRLD: Diamox tablets 125 and 250 mg) which is used to treat glaucoma, a condition in which increased pressure in the eye can lead to gradual loss of vision. The product will be manufactured at the group’s Baddi facility in Himachal Pradesh. The drug has annual sales of USD 16 million in the US as per IQVIA MAT Dec 22. Also, the company has received final approval to manufacture and market Carbidopa and Levodopa tablets USP 10 mg/100 mg, 25 mg/100 mg, and 25 mg/250 mg (USRLD: Sinemet tablets 10 mg/100 mg, 25 mg/100 mg and 25 mg/250 mg), which is used to treat Parkinson’s disease. The product will be manufactured at SEZ Ahmedabad. It has annual sales of USD 75 million as per IQVIA MAT Dec 22. Positive read through for the stock.
  • Zydus receives final nod from the USFDA for Acetazolamide Tablets

    6 Apr 2023 , 12:04PM Zydus Lifesciences gets final USFDA nod for Acetazolamide Tablets and Carbidopa & Levodopa tablets
  • Zydus Lifesciences

    29 Mar 2023 , 11:41AM Zydus Lifesciences has received final approval for Loperamide Hydrochloride Capsules USP 2 mg (USRLD: Imodium capsules) from the USFDA. The drug is indicated for the control and symptomatic relief of acute inflammatory bowel disease. It will be manufactured at the company’s SEZ facility, at Ahmedabad. Loperamide capsules had annual sales of USD 34.7 million in the US as per IQVIA MAT Jan 23. Positive for the stock.
  • Zydus Lifesciences

    29 Mar 2023 , 11:38AM Zydus Lifesciences has received final approval for Loperamide Hydrochloride Capsules USP 2 mg (USRLD: Imodium capsules) from the USFDA. The drug is indicated for the control and symptomatic relief of acute inflammatory bowel disease. It will be manufactured at the company’s SEZ facility, at Ahmedabad. Loperamide capsules had annual sales of USD 34.7 million in the US as per IQVIA MAT Jan 23. Positive for the stock.
  • Zydus receives final nod from the USFDA for Levothyroxine Sodium for Injection

    28 Mar 2023 , 12:28PM Levothyroxine Sodium Injection indicates for the treatment of myxedema coma
  • Zydus Lifesciences

    28 Mar 2023 , 11:45AM Zydus Lifesciences has received final approval from the USFDA for Levothyroxine Sodium for injection, 100 mcg/vial, 200 mcg/vial and 500 mcg/vial and Doxepin Hydrochloride capsules. Levothyroxine is indicated for treatment of myxoedema coma. It will be manufactured at Jarod, injectable facility. Doxepin is to treat Psychoneurotic patients with depression and anxiety. This will be manufactured at Moraiya facility. Strongly positive for the stock.
  • Zydus Lifesciences

    27 Mar 2023 , 11:54AM Zydus Life has received 3 observations for a Pre-Approval Inspection (PAI) for its SEZ - 1 facility at Pharmrez, Ahmedabad. There was no data integrity concern.
  • Zydus Lifesciences

    27 Mar 2023 , 11:51AM Zydus Life has received 3 observations for a Pre-Approval Inspection (PAI) for its SEZ - 1 facility at Pharmrez, Ahmedabad. There was no data integrity concern.
  • Zydus Lifesciences

    27 Mar 2023 , 11:07AM Zydus Lifesciences
  • Zydus Life gets final USFDA nod for Lubiprostone Capsules

    24 Mar 2023 , 3:29PM Zydus Life gets final USFDA nod for Lubiprostone Capsules that is used to relieve stomach pain, bloating
  • Zydus Lifesciences

    24 Mar 2023 , 11:55AM Zydus Lifesciences Ltd. has received final approval for Doxepin Hydrochloride Capsules USP 150 mg (USRLD: Sinequan capsules) from the USFDA. It is indicated for the treatment of mental / mood problems such as depression and anxiety. It will be manufactured at Moraiya facility. It had annual sales of USD 2.11 million in the US as per IQVIA MAT Jan 23. Positive development for the company.
  • Zydus gets final nod from the USFDA for Doxepin Hydrochloride Capsules USP, 150 mg

    24 Mar 2023 , 11:21AM Zydus Life gets final US FDA nod for Doxepin Hydrochloride Capsules which are used to treat depression & anxiety
  • Zydus Lifesciences gets US FDA nod for Tofacitinib tablets

    22 Mar 2023 , 10:41AM Zydus receives final and tentative Approval from the USFDA for Tofacitinib Tablets, 5 mg and 10 mg, respectively
  • Zydus grant Orphan Drug Designation by the USFDA for ZYIL1

    21 Mar 2023 , 11:02AM Zydus Life gets USFDA Orphan Drug Designation to ZYIL1 used to treat Cryopyrin Associated Periodic Syndrome
  • Zydus Lifesciences

    13 Mar 2023 , 10:03AM Zydus Lifesciences has received final approval from the USFDA for Olanzapine Orally Disintegrating Tablets USP 5, 10, 15 and 20 mg, which is a generic of USRLD Zyprexa Zydis orally disintegrating tablets. It is used to treat mental / mood conditions such as schizophrenia and bi-polar disorder. It is also used with other drugs to treat depression. The product will be manufactured in Moraiya, Ahmedabad, facility of the company. The drug had annual sales of USD 28.3 million as of Dec 22 as per IQVIA MAT.
  • Zydus Lifesciences

    8 Mar 2023 , 11:59AM Zydus Lifesciences has received final approval from the USFDA for gRevlimid (Lenalidomide) for 2.5 mg and 20 mg strengths as well. Lenalidomide capsules are used to treat various kinds of cancers. The product will be launched shortly in the US. The drug will be manufactured at Zydus Lifesciences’ SEZ, Ahmedabad facility
  • Zydus receives final approval from the USFDA for Lenalidomide Capsules

    8 Mar 2023 , 10:20AM Lenalidomide is used to treat various types of Cancers
  • Zydus Lifesciences

    2 Mar 2023 , 3:27PM Zydus Lifesciences received final approval from the USFDA for Acylovir cream (USRLD: Zovirax Cream) These are antivirals to treat cold sores caused by fever or herpes, on the face or lips. The drug will be produced at the company’s Changodar, Ahmedabad facility. The cream had annual sales of USD 16.9 million in the US as per IQVIA MAT Dec 22. Positive read through for the stock. We have Buy rating on the shares with a PT of Rs. 572 over the next 12 months.
  • Zydus gets final USFDA nod for Acyclovir Cream

    2 Mar 2023 , 2:44PM Acyclovir Cream is used to treat symptoms of herpes simplex virus infections
  • Zydus Lifesciences

    1 Mar 2023 , 10:53AM Zydus Lifesciences has received final approval from the USFDA for a blockbuster drug called Apixaban tablets with annual market size of USD 18.88 billion. Apixaban tablets 2.5 and 5 mg, is a generic copy of the US Reference Listed Drug (RLD), Eliquis tablets produced originally by Bristol Myers and Squibb. Apixaban tablets block the clotting substances of the blood. It is an anti-coagulant. It will be manufactured from Zydus’ recently approved Moraiya plant. The company has also received final approval for Olmesartan Medoxomil and Hydrochlorothiazide tablets 20 mg/12.5 mg, 40 mg/12.5 mg, and 40 mg/25 mg, which is an RLD of Benicar HCT Tablets, which lower blood pressure and risk of a stroke or a heart attack. It will be manufactured at the company’s Ahmedabad SEZ facility.
  • Zydus Lifesciences

    27 Feb 2023 , 10:47AM Zydus Lifesciences received final approval from the USFDA for Pitavastatin tablets 1 mg, 2 mg, and 4 mg which is generic of RLD Livalo tablets. Pitavastatin is a HMG-CoA inhibitor indicated as an adjunctive therapy to diet in patients with high cholesterol. Its current market size is USD 319 million in the US as per IQVIA MAT Dec 2022 Positive for the stock.
  • Zydus gets final USFDA nod for Pitavastatin tablets

    24 Feb 2023 , 3:39PM Pitavastatin tablets are used to reduce elevated cholesterol levels
  • Zydus Lifescience

    20 Feb 2023 , 11:00AM Zydus Lifesciences has received tentative approval from the USFDA for Gabapentin (once daily) 300 mg and 600 mg and also for Canagliflozin and Metformin Hydrochloride tablets. Gabapentin tablets had annual sales of USD 90 million in the US Positive read through for the stock.
  • Zydus Life gets final US FDA nod for Sirolimus tablets

    17 Feb 2023 , 11:04AM Zydus Lifesciences receives final approval from the USFDA for Sirolimus tablets 1 mg and 2 mg
  • Zydus Lifesciences

    17 Feb 2023 , 10:46AM Zydus Lifesciences Ltd. has received final approval from the USFDA for Sirolimus tablets 1 mg and 2 mg (USRLD: Rapamune Tablets) The tablets are used to prevent rejection (anti-rejection medicine) in people above 13 years of age and older who have received a kidney transplant. It is also used to treat a rare lung disorder called lymphangioleiomyotosis, which predominantly affects women of child-bearing age. The drug will be manufactured at Moraiya. Sirolimus tablets had annual sales of USD 69 million in the US (IQVIA MAT Dec 2022). Positive.
  • Zydus Lifesciences

    16 Feb 2023 , 10:15AM Zydus Lifesciences received Tentative Approval from the USFDA to market Canagliflozin tablets (USRLD: Invokna tablets) Its an SGLT - 2 inhibitor indicated adjunct to diet and exercise to improve Glycemic control in adults with type 2 diabetes. It had annual sales of USD 660 million in the US as per IQVIA MAT Dec 2022. Positive read through for the stock.
  • Zydus Lifesciences

    15 Feb 2023 , 2:53PM Zydus Life Sciences has received tentative approval from the USFDA to market Bosentan Tablets for oral suspension 32 mg (USRLD: Tracleer tablets for oral suspension) It is indicated for the treatment of pulmonary arterial hypertension (PAH) in pediatric patients aged 3 years and older with idiopathic or congenial PAH to improve pulmonary vascular resistance (PVR). The drug will be manufactured at the group’s formulation manufacturing facility at SEZ, Ahmedabad. Bosentan Tablets for oral suspension had annual sales of USD 16 million in the US (IQVIA MAT Dec 22). Positive read through for the stock. The company has already been manufacturing other strengths of gBosentan (such as 62.5 mg and 125 mg) as an authorized generic of the original.
  • Zydus Lifesciences’ Labs Q3FY23 Results

    3 Feb 2023 , 1:28PM Zydus Lifesciences’ Labs Q3FY23 Results-: In line performance
  • Zydus Life gets tentative USFDA nod for Levomilnacipran extended-release capsules

    16 Jan 2023 , 11:00AM Levomilnacipran capsules are used to treat depression
  • Zydus Lifesciences

    12 Jan 2023 , 12:35PM Zydus Lifesciences Ltd. has received final approval from the USFDA to market Brexpiprazole tablets (USRLD: REXULTI). Zydus was one of the first ANDA applicants to submit a substantially complete ANDA with a paragraph IV certification for Brexpiprazole tablets and therefore is eligible for 180 days exclusivity of shared generic drug exclusively for Brexpiprazole tablets. The drug is an antipsychotic indicated for use as an adjunctive therapy to antidepressants for the treatment of major depressive disorder (MDD). The drug has annual sales of USD 1.55 billion in the US according to IQVIA MAT Sep 22. Our view: Highly Positive.
  • Zydus Lifesciences

    11 Jan 2023 , 9:35AM Zydus Lifesciences has received final approval from the USFDA to market Febuxostat tablets which is a generic of Uloric tablets. The drug has annual sales of USD 32 million. Our view: It is marginally positive as the generic competition is high for the drug.
  • Zydus Life gets final USFDA nod for Febuxostat tablets

    10 Jan 2023 , 2:41PM Febuxostat Tablet is used to lower high Uric acid in the blood
  • Zydus Lifesciences

    10 Jan 2023 , 11:01AM CRISIL has reaffirmed its credit rating on Zydus Lifesciences to CRISIL AA+ / Positive and is supported by sustained improvement in its financial risk profile with gross debt significantly reducing to Rs. 2,419 Cr. as of Sep 22 from Rs. 4,653 Cr as of Sep 21 due to strong cash accruals. This was driven by strong liquidity it was able to gain from the sale of its domestic animal healthcare business in Q2FY22. As a result, the debt to EBITDA has reduced to 0.4x in H1FY23. The ratings continue to reflect the established position of the Zydus group in the branded generics market in India and the expected benefits from growth in the wellness segment; the ratings also factor in its growing presence in international markets. Our view: Positive read through for the stock.
  • Zydus Lifesciences

    6 Jan 2023 , 3:16PM Zydus Lifesciences’ subsidiary Zydus Pharmaceuticals Ltd. (USA) Inc. (Zydus) has launched Topiramate Extended-Release Capsules. The company had earlier received final approval from the USFDA to market Topiramate Extended-Release capsules USP 25 mg, 50 mg, 100 mg, (USRLD: Trokendi XR). It is indicated for Epilepsy. It had annual sales of USD 488 million in the US as per IQVIA MAT Nov 2022 data. Our view: Highly positive for the company as with no generic competition as of now.
  • Zydus Lifesciences

    6 Jan 2023 , 12:59PM Zydus Lifesciences’ subsidiary Zydus Pharmaceuticals Ltd. (USA) Inc. (Zydus) has launched Topiramate Extended-Release Capsules. The company had earlier received final approval from the USFDA to market Topiramate Extended-Release capsules USP 25 mg, 50 mg, 100 mg, (USRLD: Trokendi XR). It is indicated for Epilepsy. It had annual sales of USD 488 million in the US as per IQVIA MAT Nov 2022 data.
  • Zydus Life arm launches Topiramate extended-release capsules in US

    6 Jan 2023 , 12:38PM Topiramate capsule is used to treat Epilepsy
  • Zydus Lifesciences

    2 Jan 2023 , 12:44PM Zydus Lifesciences received final approval from the USFDA to market Triazolam tablets USP, 0.125 mg and 0.25 mg (USRLD: HALCION tablets), which are used in a short term to treat insomnia. The drug will be manufactured at Moraiya, Ahmedabad, India. The tablets had annual sales of USD 11.7 million in the US as per IQVIA data (IQVIA MAT Sep 22). Our view: Marginally positive.
  • Zydus Lifescience

    23 Dec 2022 , 9:04AM Zydus Lifesciences received final approval from the USFDA with 180 days exclusivity for Selexipag tablets in 200 mcg, 400 mcg, 600 mcg, 800 mcg, 1,000 mcg, 1,200 mcg, 1,400 mcg, 1,600 mcg (RLD: Uptravi tablets) The tablets are indicated for treatment of pulmonary arterial hypertension. The drug will be manufactured at the company’s Ahmedabad SEZ, India. Selexipag tablets have an annual market size of USD 577 million in the US according to IQVIA data as of Sep 22. Our view: Positive as Zydus emerges as the first generic producer of it with 180 days exclusivity to it.
  • Zydus Lifesciences

    12 Dec 2022 , 10:02AM Zydus receives two final generic product approvals from the USFDA for Silodosin and Pregabalin capsules. The drugs will be manufactured at the group’s formulation manufacturing facility at Moraiya, Ahmedabad, India. Silodosin capsules which is indicated for treating prostate gland had annual sales of USD 14 million in the United States and Pregabalin capsules, which are indicated for treating nerve pain out of spinal cord injury had annual sales of USD 242 million, according to IQVIA data (IQVIA MAT Sep 2022)
  • Zydus gets final nod from USFDA for Estradiol Transdermal System

    2 Dec 2022 , 12:09PM Zydus receives final approval from the USFDA for Estradiol Transdermal System which will be manufactured at the Moraiya plant
  • Zydus Life gets final USFDA nod for Topiramate Extended-Release Capsules

    1 Dec 2022 , 10:37AM Topiramate Extended-Release Capsules are used to control seizures in people with Epilepsy
  • Zydus Life to purchase business undertakings of Watson Pharma for Rs. 46.8 cr

    29 Nov 2022 , 2:18PM Zydus Lifesciences enters into a BTA for purchase of one of the Business Undertakings
  • Zydus Life receives tentative approval from the USFDA for Levothyroxine Sodium for injection

    28 Nov 2022 , 10:23AM Levothyroxine Sodium injection is used to treat Myxedema Coma
  • Zydus Lifesciences

    28 Nov 2022 , 9:10AM Zydus Lifesciences: The company receives tentative approval from the USFDA for Levothyroxine Sodium for Injection. Levothyroxine Sodium injection had annual sales of USD 45.2 mn in the United States according to IQVIA data (IQVIA MAT Sep 2022). The group now has 334 approvals and has so far filed over 431 ANDAs since the commencement of the filing process in FY 2003-04 – Positive read through for the stock.
  • Zydus Lifesciences

    16 Nov 2022 , 12:38PM The company has received exclusive marketing rights for CanAssist Breast- an innovative prognostic test for breast cancer patients. The test brings in 95% precision in gauging whether hormone positive breast cancer patients need chemotherapy or not. This will benefit patients and clinicians pan India with a highly accurate and an evidence based approach for breast cancer treatment. CanAssist Breast is a patented product of OncoStem, a research based startup headquartered in Bengaluru. With this new offering, Zydus has expanded its offerings to include prognostic and diagnostic approaches that can greatly benefit cancer patients and clinicians. Positive read thru.
  • Zydus Lifesciences

    25 Oct 2022 , 10:19AM The company has received final approval from the USFDA to market Ketorolac Tromethamine Tablets USP, 10 mg. Ketorolac Tromethamine Tablets are indicated to relieve moderately severe pain, usually after surgery. The drug will be manufactured at the group’s formulation manufacturing facility at Ahmedabad SEZ. Ketorolac Tromethamine Tablets had annual sales of USD 17mn in the United States according to IQVIA data (IQVIA MAT Aug 2022). Positive for the stock.
  • Zydus Lifescience

    17 Oct 2022 , 2:43PM The company’s subsidiary, Zydus Worldwide DMCC, has received tentative approval from the USFDA to market Valbenazine Capsules USP 40mg, 60mg, and 80mg. Valbenazine Capsules are indicated for the treatment of adults with tardive dyskinesia (movements in the face, tongue, or other body parts that cannot be controlled). The drug will be manufactured at the group’s formulation manufacturing facility at Ahmedabad SEZ. Valbenazine Capsules had annual sales of USD 781mn in the United States according to IQVIA data (IQVIA MAT Aug 2022). Positive for the stock.
  • Zydus Lifesciences

    6 Oct 2022 , 10:58AM The company has received final approval from the USFDA to market Brivaracetam Tablets USP 10mg, 25mg, 50mg, 75mg, and 100mg. Zydus was one of the first ANDA applicants to submit a substantially complete ANDA with a paragraph IV certification for Brivaracetam Tablets USP 10 mg, 25 mg, 50 mg, 75 mg, and 100 mg. It is therefore eligible for 180 days of shared generic drug exclusivity for Brivaracetam Tablets USP 10mg, 25mg, 50mg, 75mg, and 100mg. Brivaracetam is indicated for the treatment of partial-onset seizures in patients 4 years of age and older. The drug will be manufactured at the group’s formulation manufacturing facility at Ahmedabad SEZ. Brivaracetam Tablets USP 10mg, 25mg, 50mg, 75mg, and 100mg had annual sales of USD 412 mn in the United States according to IQVIA data (IQVIA MAT August 2022). Positive for the stock
  • Zydus Life gets tentative USFDA nod for Amantadine Capsules

    4 Oct 2022 , 2:25PM Amantadine capsules is used to treat Parkinson's disease
  • Zydus Lifesciences

    3 Oct 2022 , 10:36AM The company has received approval from the USFDA to market Sildenafil, the high blood pressure drug (pulmonary hypertension). It works by relaxing and widening the blood vessels in lungs which allows the blood to flow more easily. The drug will be manufactured at the group’s formulation manufacturing facility at Baddi, Himachal Pradesh. The drug had annual sales of $65 million in the United States according to IQVIA data of August 2022 - Positive for the stock.
  • Zydus Life gets final USFDA nod to market Mirabegron tablets

    3 Oct 2022 , 10:24AM Zydus Life gets 180 days shared exclusivity, final USFDA nod to market Mirabegron tablets
  • Zydus Lifescience

    21 Sep 2022 , 11:08AM BridgeBio Pharma, Inc. (BridgeBio) and Sentynl Therapeutics Inc. (owned by Zydus Lifesciences; Sentynl), announced that the European Commission (EC) has granted marketing authorization for NULIBRY® (fosdenopterin) as the first therapy for the treatment of patients with molybdenum cofactor deficiency (MoCD) Type A. European Commission (EC) decision is based on the efficacy and safety data collected to date compared to data from a natural history study. NULIBRY was BridgeBio’s first FDA-approved therapeutic; Sentynl acquired global rights of NULIBRY in March 2022 – Positive read through for Zydus Lifesciences
  • Zydus Lifesciences

    20 Sep 2022 , 2:23PM The company has launched Lenalidomide Capsules in the US. It received final approvals for 5 mg, 10 mg, 15 mg and 25 mg strengths and tentative approvals for 2.5 mg and 20 mg strength USRLD: Revlimid. Lenalidomide is used to treat various types of cancers. It works by slowing or stopping the growth of cancer cells. It is also used to treat anemia in patients with certain blood/bone marrow disorders (myelodysplastic syndrome-MDS). The drug is being manufactured at the group’s formulation manufacturing facility at Ahmedabad SEZ, India. The product had annual sales of USD 2.86 bn (~Rs2200crore) in the United States, according to IQVIA MAT in July 2022 – Positive read through for the stock.
  • Zydus life launches Lenalidomide capsules in the US

    20 Sep 2022 , 2:03PM Lenalidomide is used to treat various types of cancers & anemia
  • Zydus Lifesciences

    16 Sep 2022 , 2:50PM The company’s US subsidiary has received tentative approval from the USFDA to market Sugammadex Injection USP strength - 200 mg/2 mL (100 mg/mL) and 500 mg/5 mL (100 mg/mL), Single-Dose Vial. Sugammadex is indicated for the reversal of neuromuscular blockade. The drug will be manufactured at the group’s injectables manufacturing facility at Jarod, India. Sugammadex injection had annual sales of USD 772 million in the US according to IQVIA MAT July 2022. Considering the tentative approval, the product could be launched post receipt of final approval, hence long-term positive.
  • Zydus receives tentative approval from the USFDA for Sugammadex Injection

    16 Sep 2022 , 12:59PM Sugammadex injection is used to reverse the effects of muscle relaxants
  • Zydus Life Science

    14 Sep 2022 , 11:04AM Zydus Life Science: Gets USFDA approval for Lenalidomide Capsules – strength 2.5 mg, 5 mg, 10 mg, 15 mg, 20 mg, and 25 mg. The company has received final approvals for strengths 5 mg, 10 mg, 15 mg and 25 mg and tentative approvals for 2.5 mg and 20 mg strength. Lenalidomide is used to treat various types of cancers. It works by slowing or stopping the growth of cancer cells. It is also used to treat anemia in patients with certain blood/bone marrow disorders. Lenalidomide capsules had annual sales of USD 2.86 bn in the United States, which is substantial. Positive read through
  • Zydus Life gets final USFDA nod for Lenalidomide capsules

    13 Sep 2022 , 12:21PM Lenalidomide is used to treat various types of cancers
  • Zydus gets final nod and 180 days shared exclusivity from the USFDA for Cariprazine Capsules

    12 Sep 2022 , 2:07PM Cariprazine Capsules is used to treat Depression
  • Zydus in-licenses a critical drug for CKD patients from Pharmacosmos A/S of Denmark

    9 Sep 2022 , 10:36AM Acquires right to market MonoFerric injections in India from Denmark's Pharmacosmos A/S
  • Zydus get final USFDA nod for Prochlorperazine Maleate tablets

    11 Aug 2022 , 10:33AM Prochlorperazine Maleate Tablet is used to treat severe nausea & vomiting
  • Zydus Lifesciences

    8 Aug 2022 , 9:56AM The USFDA has inspected the company’s Moraiya manufacturing plant from 26th July to 5th August 2022. The inspection ended with form 483 being issued with 4 observations. None of this observations relate to data integrity issues and the management is confident of replying to the regulators a stipulated time frame. Stock to remain in focus.
  • Zydus Lifesciences

    4 Aug 2022 , 12:52PM Zydus Life Sciences: Gets Final approval from the USFDA for Ivermectin Cream, 1%, used for the treatment of inflammatory lesions of rosacea. Ivermectin Cream had annual sales of $176 million in the US as per IQVIA MAT June 2022. Also Zydus Life Sciences gets USFDA approval Empagliflozin Tablets USP 10 mg and 25 mg. Empagliflozin is used to lower blood sugar levels in people with type 2 diabetes. Itis also used to reduce the risk of stroke, heart attack, or death in people with type 2 diabetes along with heart and blood vessel disease. Empagliflozin Tablets had annual sales of $9.8 bn in the US as per IQVIA MAY June 2022. Given the substantial addressable market size the approvals are positive
  • Zydus receives final approval from the USFDA for Empagliflozin Tablets

    4 Aug 2022 , 12:25PM Empagliflozin is used to lower blood sugar levels in people with type 2 diabetes
  • Zydus Lifesciences gets final nod from the USFDA for Ivermectin Cream

    4 Aug 2022 , 12:13PM Ivermectin Cream is a used for the treatment of inflammatory lesions of rosacea
  • Zydus Lifesciences

    21 Jul 2022 , 10:16AM Zydus Lifesciences: gets final approval from the USFDA Norepinephrine Bitartrate Injection USP,4 mg/4 mL Single-Dose Vial. The drug is indicated for treating blood pressure in adult patients with acute hypotensive state. Norepinephrine Bitartrate Injection USPhad annual sales of US$ 63.8 million in the US. Positive
  • Zydus Lifesciences

    19 Jul 2022 , 10:26AM Subsidiary Zydus Worldwide DMCC has received final approval from the USFDA for Efinaconazole Topical Solution, 10%. Efinaconazole is an azole antifungal used for the topical treatment of Onychomycosis of the toenails. The reference listed drug - Jublia had annual sales of $292 million in the United States and basis this the approval is positive
  • Zydus Life gets final USFDA nod for Efinaconazole Topical solution

    18 Jul 2022 , 3:43PM Zydus receives final approval from the USFDA for Efinaconazole Topical Solution
  • Zydus Lifesciences

    11 Jul 2022 , 10:53AM Zydus Lifesciences: has launched the molecule Sitagliptin in India under the brand names Sitaglyn and Siglyn to address Type 2 diabetes in India. Both the brands will add on to a comprehensive solution for the management of Type 2 diabetes at an affordable cost, which is around 60% lesser than the originator’s cost. Both the drugs belong to the DPP4 inhibitor category with a 62% global market share and the drug is very effective in controlling HbA1C levels. Positive
  • Zydus Life receives final nod from US FDA for Empagliflozin & Metformin Hydrochloride tablets

    11 Jul 2022 , 10:33AM Tablets used to lower the risk of cardiovascular death in patients with type 2 diabetes mellitus
  • Zydus Lifescieces

    14 Jun 2022 , 10:59AM Zydus Lifesciences: The company had announced a buy back offer for buying back 1.15 cr equity shares amounting to Rs 750 cr at a price of Rs 650 per share. The company has announced 23 June 2022 and July 06, 2022 as the opening and closing dates for the offer respectively.
  • Zydus Lifesciences

    7 Jun 2022 , 9:49AM Gets USFDA approval for Adapalene and Benzoyl Peroxide Topical Gel, which is a combination drug. The gel is used to decrease the number and severity of acne pimples. The Adapalene and Benzoyl Peroxide Topical Gel had a market size of $195 mn. Given the healthy addressable market size the approval is positive
  • Zydus Lifesciences receives final approval from USFDA for Famotidine Tablets

    6 Jun 2022 , 9:56AM Famotidine Tablets, used to prevent and treat heartburn and other symptoms caused by excessive acid in the stomach
  • Zydus Lifesciences

    30 May 2022 , 9:33AM The company has received an EIR (Establishment Inspection Report) from the USFDA for iits Injectables manufacturing facility at Jarod. The USFDA has determined that the inspection classification as Voluntary Action Indicated (VAI) and has concluded that the inspection is considered as Closed. The inspection was a Pre-Approval cum cGMP inspection and it covered 15 ANDAs. The receipt of the EIR is positive and the company would now be able to launch injectables products in the US markets from this Facility
  • Zydus Lifescience Q4FY22 results

    20 May 2022 , 2:56PM Zydus Lifescience Q4FY22 results – weak Q4; operating performance misses estimates, board approves buyback proposal
  • Zydus Lifesciences

    18 May 2022 , 2:18PM A meeting of the board of directors of the company is scheduled on 20 May 2022 and and the board shall also consider a proposal for buy back of its fully paid up equity shares.
  • Zydus Lifesciences board to mull buyback

    18 May 2022 , 12:35PM Board to consider Buyback of Equity Shares
  • Zydus Lifesciences

    13 May 2022 , 10:22AM Zydus Lifesciences: has launched Bemdac, for the first time in India. The drug in a new line of treatment for patients suffering from uncontrolled levels of LDL-Cholesterol despite life-style modifications and the use of maximum tolerated dose of statins. According to studies, 8 out of 10 Indians are dyslipidemic1 and 112 million adults suffer from high levels of LDL-Cholesterol, thus pointing at a sizeable addressable market in India. Positive
  • Zydus receives tentative approval from USFDA for Selexipag Tablets

    6 May 2022 , 1:45PM Selexipag Tablet is used to treat Pulmonary Arterial Hypertension
  • Aurobindo, Zydus Lifesciences

    4 May 2022 , 9:44AM Eugia Pharma Specialties Limited a subsidiary of Aurobindo and Zydus Lifesciences, has received a final approval from the USFDA for Bortezomib for injection, 3.5 mg, which is indicated for treatment of Adult patients with multiple myeloma and mantle cell lymphoma, which are types of cancers. The product is a bioequivalent and therapeutically equivalent to the Velcade for Injection, which has a market size of US$ 1172 million for the twelve months ending March 2022. Given the substantial addressable market size the product approval is positive.
  • Zydus Lifesciences

    27 Apr 2022 , 3:18PM Gets DCGI emergency use approval for its Covid Vaccine Zycov-D for the two dose regimen. With the approval, the drug can be administered as a 3 mg two-dose inoculation schedule for population aged 12 years and above and can be administered within a gap of 28 days. Positive read thru
  • Zydus Lifesciences

    13 Apr 2022 , 12:34PM Zydus Lifesciences: Has announced that it would be manufacturing and supplying Sagent’s Caffeine Citrate Oral Solution in the strength of 60 mg per 3 mL from its injectables facility at Jarod, Gujarat. The announcements is after the company receiving PAS (Prior Approval Supplement) approval from the USFDA which allows for a site transfer and manufacturing of the drug at Jarod. The drug is indicated for treating short term breathing problems in premature infants. Positive read through as the site transfer approval from the USFDA could have a positive rib off effect for other products which are stuck up at plant yet to be cleared by regulatory agencies.
  • Zydus Life to manufacture & supply Sagent’s Caffeine Citrate Oral Solution

    13 Apr 2022 , 12:02PM Zydus to supply Sagent's Caffeine Citrate Oral Solution from Jarod, post USFDA's PAS Approval
  • Zydus Lifesciences

    11 Apr 2022 , 11:06AM As per media news, Cadila Pharmaceuticals has developed a world’s first novel three-dose vaccine to treat rabies. The vaccine developed by the company is a three dose regimen as against the 5 dose vaccines available currently. The vaccine has been approved by the regulator DCGI and the company would be launching it in 11 states, including Gujarat in the first phase. The cost of vaccine has been fixed at Rs 750 per vial and the full treatment cost is expected to be Rs 2145. Also considering that the vaccine has advantage over existing ones being a three dose regimen, The approval and subsequent launch could be positive read thru
  • Stock Update: Zydus Lifesciences

    8 Apr 2022 , 11:34AM Stock Update: Zydus Lifesciences - US performance to be strained in near term; India outlook stays strong
  • Zydus Lifesciences

    22 Mar 2022 , 11:18AM Zydus Lifesciences (earlier Cadila Healthcare): Cyprium Therapeutics, Inc with support from its licensing partner Sentynl Therapeutics, which is a wholly owned subsidiary company of Zydus Lifesciences, announced positive data on CUTX-101with respect to safety and efficacy in patients with Menkes disease. As Menkes disease is a rare paediatric disease, CUTX-101 has been granted a orphan drug designations and hence the positive data from the development stages bodes well for Zydus Lifesciences and is a potential positive.
  • Zydus gets prior approval supplement (PAS) nod from USFDA for Mycophenolate Mofetil for Injection USP

    21 Mar 2022 , 10:06AM Mycophenolate Mofetil is indicated for use in combination with other drugs
  • Zydus Life Sciences

    9 Mar 2022 , 9:46AM Zydus Lifesciences (earlier known as Cadila): Sentynl Therapeutics, Inc, a wholly owned subsidiary company announced the execution of an asset purchase agreement to buy BridgeBio’s NULIBRY (injection). The injection is approved by the USFDA to reduce the risk of mortality in patients with molybdenum cofactor deficiency (MoCD) Type A, an ultra-rare, life-threatening paediatric genetic disorder. Under the terms of the Agreement, Sentynl will acquire global rights to NULIBRY and will be responsible for the ongoing development and commercialisation of NULIBRY in the United States and developing, manufacturing and commercialising it globally. Being a rare and an orphan disease, the asset acquisition would add to Zydus Lifesciences’ specialty drugs portfolio, which points at substantial growth going ahead, hence positive
  • Zydus receives final approval from USFDA for Dapagliflozin Tablets

    23 Feb 2022 , 12:28PM Cadila Health's Zydus gets USFDA nod for Dapagliflozin tablets, used to treat chronic kidney disease & used to lower the risk of heart failure in adults
  • Cadila Healthcare

    21 Feb 2022 , 11:33AM Cadila Healthcare: The board of directors of the company in the Extra Ordinary general meeting have approved the change of name of the company from “Cadila Healthcare” to “Zydus Lifesciences Limited”. The change in name is unlikely to have any material impact on the financials of the company
  • Cadila Healthcare

    14 Feb 2022 , 9:38AM Cadila: US Subsidiary gets final approval from the USFDA to market Roflumilast Tablets in the strength of 500 mcg and a tentative approval for Roflumilast Tablets, 250 mcg. Zydus being one of the first applicants for Roflumilast Tablets, 500 mcg is eligible for 180 days of shared generic drug exclusivity. Roflumilast Tablets are indicated as a treatment to reduce the risk of chronic obstructive pulmonary disease (COPD) exacerbations in patients with severe COPD associated with chronic bronchitis. Given the 180 day exclusivity the approvals are positive.
  • Stock Update: Cadila Healthcare Q3FY22 Results

    4 Feb 2022 , 12:32PM Stock Update: Cadila Healthcare Q3FY22 Results - Steady Q3; India, Emerging markets to be growth drivers
  • Cadila Healthcare Q3FY22 results

    3 Feb 2022 , 4:15PM Cadila Healthcare Q3FY22 results – Steady quarter; higher other income led to PAT marginally ahead of estimates
  • Zydus receives final approval from USFDA for Vigabatrin Tablets

    20 Jan 2022 , 11:11AM Cadila Health gets USFDA nod to market Vigabatrin tablets, used to treat children with infantile spasms
  • Cadila Healthcare receives tentative nod from USFDA for Pimavanserin capsules

    31 Dec 2021 , 3:02PM Pimavanserin is use for the treatment of hallucinations and delusions associate with Parkinson's disease psychosis
  • Stock Update: Cadila Healthcare

    29 Dec 2021 , 10:07AM Stock Update: Cadila Healthcare - On a healthy growth path; Price correction provides an opportunity
  • Stock Update: Cadila Healthcare

    29 Dec 2021 , 10:05AM Stock Update: Cadila Healthcare - On a healthy growth path; Price correction provides an opportunity
  • Cadila Healthcare

    23 Dec 2021 , 11:27AM Gets tentative USFDA approval for Pimavanserin tablets in strength of 10 mg. Pimavanserin is used to treat the symptoms of a certain mental or mood disorder known as Psychosis that might occur with Parkinsons. Positive read thru as the tentative approval could widen the US products portfolio, once launched.
  • Zydus Cadila receives tentative approval from USFDA for Pimavanserin Tablets

    22 Dec 2021 , 12:42PM Pimavanserin tablet is use to treat Parkinson's disease psychosis
  • Cadila Healthcare

    16 Dec 2021 , 2:39PM Cadila: Gets Orphan drug designation from the USFDA for its novel drug - ZY-19489, a compound to treat malaria. Orphan drug designation provides eligibility for certain development incentives, including tax credits for qualified clinical testing, prescription drug user fee exemptions and seven-year marketing exclusivity upon FDA approval. ZY-19489 is a potential single dose radical cure for P. falciparum and P. vivax malaria which is a major global health risk. This is a long term potential positive, subject to getting the required regulatory approvals.
  • USFDA gives an orphan drug designation a novel compound to treat malaria

    16 Dec 2021 , 11:31AM Zydus receives Orphan Drug Designation from US FDA for ZY-19489, a novel compound to treat malaria
  • Cadila Healthcare

    14 Dec 2021 , 10:09AM To roll out its Covid Vaccine ZyCov-D to be included in the vaccination drive and would be the fourth vaccine to be a part of the Governments vaccination program. The Government would start giving the vaccine shots commencing next week. Initially the vaccine would be introduced in the following seven states - Bihar, Jharkhand, Maharashtra, Punjab, Tamil Nadu, Uttar Pradesh and West Bengal and would be given to adult population. The company has already received an order to supply 1 cr dosses to the Government of India and further it expects to manufactures 4-5 crore doses by January 2022.The launch of the vaccine offers substantial growth opportunity and sizeable manufacturing capacity for vaccine bodes well; hence positive.
  • Cadila Healthcare

    13 Dec 2021 , 10:49AM Cadila: Gets tentative approval from the USFDA for Cariprazine Capsules in the strengths of 1.5 mg, 3 mg and 4.5 mg, and 6 mg fir the US markets. Cariprazine Capsules are indicated for the treatment of schizophrenia and acute treatment of manic or mixed episodes associated with bipolar disorder. The tentative approval is positive as it would widen the product portfolio for the US markets.
  • Zydus to begin Phase II (a) clinical trial of ZYIL1

    13 Dec 2021 , 10:09AM Zydus to begin Phase II (a) clinical trial of ZYIL1, a novel oral NLRP3 inflammasome inhibitor in patients
  • Zydus gets USFDA nod for next phase trial of Saroglitazar in patients with Cholangitis

    10 Dec 2021 , 9:56AM Zydus announces EPICS-IIITM Phase 2(b)/3 adaptive pivotal clinical trial of Saroglitazar Magnesium in PBC
  • Cadila Healthcare

    7 Dec 2021 , 11:02AM The company’s Covid Vaccine - ZyCov-D is likely to be rolled out in the state of West Bengal by mid December 2021. The vaccine is a fourth one to be included in the nationwide inoculation drive and is a three dose regimen. Positive read thru
  • Cadila Healthcare

    3 Dec 2021 , 11:01AM As per media news the Government of India would initially introduce Covid Vaccine ZyCov-D in 7 states including West Bengal and Maharashtra. The company will supply 1 crore doses of ZyCoV-D to the Government of India and is also the first needle free, painless vaccine for Covid. Positive Read thru.
  • Cadila Healthcare

    25 Nov 2021 , 10:29AM Has entered in to a licensing manufacturing and technology transfer agreement with Enzyme Lifesciences – Republic of Korea based company for its Covid Vaccine ZyCov-D. Cadila will provide manufacturing license and transfer the Plasmid DNA vaccine technology to Enzychem Lifesciences and in turn Enzymes Lifesciences would manufacture and commercialize the vaccine in its territory and Cadila would receive the license fees and royalty payments for the same. Positive read thru
  • Cadila submits NDA for treatment of anaemia

    23 Nov 2021 , 10:42AM Zydus develops new treatment for patients suffering from Chronic Kidney Disease, submits first NDA to DCGI
  • Cadila Healthcare

    22 Nov 2021 , 11:51AM Cadila: gets USFDA approval for Decitabine for Injection in the strength of 50 mg/vial Single-Dose Vial for the US markets. The injection is used to treat Myelodysplastic Syndrome and certain types of blood or bone marrow cancery. The approval would widen the company’s offerings in the US markets and could aid topline growth, hence positive
  • Cadila Healthcare

    18 Nov 2021 , 9:42AM As per media reports, the company gets USFDA approval for Nelarabine Injection, which is used to treat certain types of cancer like leukemia and lymphoma, for the US markets. Also Cadila has received a 180 day exclusivity for the injection. Given the 180 day exclusivity, the product approval is positive.
  • Cadila Healthcare

    12 Nov 2021 , 3:00PM Cadila: gets USFDA tentative approval for Eluxadoline Tablets in the strengths of 75 mg and 100 mg, which are indicated for the treatment of irritable bowel syndrome with diarrhea. The receipt of tentative approval is positive as it would widen the product basket for the US markets
  • Zydus Cadila receives tentative approval from USFDA for Eluxadoline Tablets

    12 Nov 2021 , 11:09AM Cadila Health receives tentative approval from USFDA for Eluxadoline Tablets, used for treatment of irritable bowel syndrome with diarrhea
  • Zydus Cadila receives final approval from USFDA for Glycopyrrolate Injection

    10 Nov 2021 , 12:32PM Glycopyrrolate is use before surgery to decrease the volume of secretions from mouth, lungs and stomach
  • Cadilla Healthcare

    8 Nov 2021 , 9:55AM As per media reports, the Government of India has placed an order to purchase 1cr doses of the company’s Covid vaccine – ZyCov-D at a price of Rs 358 per dose. The vaccine is the first one to be approved for the age group 12-18 years of population and offers a sizeable potential for Cadila, hence positive
  • Cadila Healthcare

    11 Oct 2021 , 10:54AM Announced positive results from an efficacy and safety analysis from completion of two patient studies for CUTX-101 - copper histidinate, which is being evaluated to treat Menkes disease. Treatment with CUTX101 demonstrated a significantly greater median overall survival, which bodes well. Cadila’s wholly owned Sentynl, is a marketing partner for the drug, which is being developed by Cyprium Therapeutics. Positive for Cadila if the drug gets successfully approved
  • Cadila Healthcare

    8 Oct 2021 , 12:35PM Cadila: gets USFDA tentative approval for Adapalene and Benzoyl Peroxide Gel - 0.3%/2.5%, which ius used to treat acne. The product would be manufactured at the groups Topical plant at Ahmedabad. The tentative approval would widen the product offerings in the US markets, hence positive.
  • Zydus Cadila gets tentative USFDA nod for Adapalene & Benzoyl Peroxide gel

    8 Oct 2021 , 12:29PM Adapalene and Benzoyl Peroxide combination is used to treat acne
  • Cadila Healthcare

    5 Oct 2021 , 11:00AM As per media reports, the company’s Covid vaccine – ZyCov-D is likely to be launched by mid October as against the earlier plans to roll out by October. The delay could be due to on-going price negotiations for the vaccine between the company and Government, which are awaited.
  • Cadila Healthcare

    4 Oct 2021 , 10:59AM The Indian drug regulator has given permission for conducting Phase III trial on the two-dose regimen of its needle-free Covid-19 vaccine, ZyCoV-D, which currently has been approved as a three dose regimen. Positive if the trials and successfully completed and the 2-dose vaccine gets approved. Also the company has proposed a pricing of Rs 1900 for the 3 dose vaccine which can be administered on people above 12 years of age. However the government is negotiating for a reduction in price and a final decision on it is likely to be taken this week.
  • Cadila Healthcare

    27 Sep 2021 , 10:46AM As per media news, the company’s Covid vaccine – ZyCoV-D is in the process to be included in the Governments inoculation programme. However, the pricing is a clear issue and the decision is likely to be expected soon. If the vaccine becomes a part of the Government’s vaccination program, then it could drive the volumes upwards, though pricing clarity is awaited. Sentimentally positive.
  • Zydus Cadila gets USFDA nod for psoriasis drug Apremilast tablets

    24 Sep 2021 , 11:09AM Zydus Cadila receives final approval from USFDA for Apremilast Tablets
  • Cadila Healthcare unit inks pact to sell two brands to Integrace

    21 Sep 2021 , 11:02AM Cadila Healthcare arm inks pact with Integrace Pvt Ltd to sell two brands -- Mifegest and Cytolog
  • Cadila Healthcare

    21 Sep 2021 , 9:36AM Cadila Healthcare: pact with Intergrace to sell Mifegest and Cytolog brands-positive read-thru
  • Cadila Healthcare

    20 Sep 2021 , 9:40AM Cadila Healthcare- Received final approval from the USFDA to market Vortioxetine Tablets- Positive read-through.
  • Cadila Healthcare

    9 Sep 2021 , 2:19PM Cadila: Gets tentative approval from the USFDA to market Brexpiprazole Tablets in the strength of 0.25 mg, 0.5 mg, 1 mg, 2 mg, 3 mg, and 4 mg. Brexpiprazole is an atypical antipsychotic indicated for use as an adjunctive therapy to antidepressants for the treatment of Major Depressive Disorder (MDD) and for treatment of schizophrenia. The approval is positive as it would add to the growth of the US sales.
  • Zydus Cadila gets tentative approval from the USFDA to market Brexpiprazole Tablets

    9 Sep 2021 , 12:00PM Zydus Cadila receives tentative approval from the USFDA to market Brexpiprazole Tablets in the strength
  • Cadila Healthcare

    6 Sep 2021 , 1:53PM Cadila: Subsidiary company has got a tentative approval from USFDA for new drug application for Sitagliptin base 25, 50 and 100 mg tablets. On 31 October 2020 the company had filed a New Drug Application (NDA) under Section 505(b) with the USFDA for seeking approval to market Sitagliptin. The company received the tentative approval upon completion of the first review cycle on 2 September 2021. The receipt of the tentative approval is positive.
  • Zydus Cadila's Sitagliptin base tablets gets Tentative Approval from FDA

    6 Sep 2021 , 10:48AM Zydus' Sitagliptin base contains the active moiety Sitagliptin in a different form
  • DR Reddys, Cadila Healthcare

    30 Aug 2021 , 10:57AM Both the companies are recalling drugs in the US markets. Dr Reddys is recalling 37560 bottles of Tizanidine HCl tablets, USP 4mg due to Failed Tablet/Capsule Specification as some tablets were shaved while Cadila’s arm – Zydus Pharmaceuticals (USA) is recalling 2880 bottles of Carevdilol tablets USP – 25 mg due to presence of foreign tablets/ capsules; there were two Paroxetine tablets found in the bottle. Both the recalls are classified as class II recalls by the USFDA and hence is unlikely to have any material impact on the financial performance of the companies.
  • Cadila Healthcare

    23 Aug 2021 , 12:54PM Cadila: gets final approval from the USFDA for Tofacitinib extended release tablets strength - 11 mg and 22 mg. The drug is used to treat psoriatic arthritis and rheumatoid arthritis and is also used to reduce symptoms of ulcerative colitis. Tofacitinib extended-release tablets had annual sales of approximately $2082 million in US for the year ending June 2021 according to IQVIA. Also the company has a 180 day exclusivity on the tablet with the 22 mg strength. Given the sizeable addressable market size and 180 days exclusivity, points at a strong growth potential for the US business (~43% of FY21 sales) and hence is Positive.
  • Zydus Cadila gets 180-day exclusivity for Tofacitinib extended release 22 mg tablets

    23 Aug 2021 , 11:21AM Zydus Cadila gets 180-day exclusivity for Tofacitinib extended release 22 mg tablets, announces final approval from USFDA
  • Cadila Healthcare

    23 Aug 2021 , 9:33AM Cadila: The company has received an Emergency Use Approval form the DCGI for its Plasmid DNA Vaccine for COVID-19 – ZyCoV-D, which is a three dose vaccine. The vaccine is available for adolescents in the 12-18 age group, besides the adult population as well. The company plans to manufacture 10-12 crore doses of ZyCoV-D annually. The pricing of the vaccine would be announced in the next 1-2 weeks and the company plans to supplies to start by middle to end of September 2021. The approval of the vaccine is positive as it points towards a strong growth potential for Cadila.
  • Cadila Health signs licence & supply agreement with CHEMI SpA of Italy

    20 Aug 2021 , 12:40PM Zydus partners with CHEMI of Italy to launch Enoxaparin Sodium Injection in the United States
  • Cadila Healthcare

    18 Aug 2021 , 9:37AM Cadila: Gets tentative approval from the USFDA for Lenalidomide Capsules in the strengths of 2.5 mg, 5 mg,10 mg, 15 mg, 20 mg, and 25 mg. Lenalidomide capsules are used to treat various types of cancers and is also used to treat anemia in patients with certain blood/bone marrow disorders. The drug would be manufactured at the company’s SEZ plant at Ahemdabad and the tentative approval is positive as it would widen the product basket in the key market of US.
  • Cadila Healthcare

    13 Aug 2021 , 1:46PM Cadila: Gets final approval from the USFDA to market Mesalamine Extended-Release Capsules in the strength of 0.375 g, indicated for maintenance of remission of ulcerative colitis in adults patients. The drug would be manufactured at the Sez facility at Ahmedabad. Approval is positive as it would add to the US topline growth which constitutes around 43% of the overall sales.
  • Zydus Cadila receives final approval from USFDA for Mesalamine Extended-Release Capsules

    13 Aug 2021 , 11:16AM Mesalamine extended-release capsules use to treat ulcerative colitis
  • Cadila Healthcare: Stock update

    12 Aug 2021 , 11:42AM Cadila Healthcare: Stock update - Steady Q1; eyeing a growth sweet spot
  • Cadila Healthcare: First Cut - Q1FY22

    11 Aug 2021 , 3:29PM Cadila Healthcare: First Cut - Q1FY22 – Healthy quarter; Numbers in line with estimates
  • Cadila Healthcare

    10 Aug 2021 , 10:37AM As per media reports the company’s Covid Vaccine – ZyCov-D is expected to get an emergency approval from the indian drug regulator. ZyCov-D is a three dose vaccine and the company has applied for an emergency use in the previous month. Initially the approval is expected to adults while the DCGI is examining the vaccine for Childern as well. If approved could be positive as it would open up sizeable potential growth opportunities.
  • Cadila Healthcare

    30 Jul 2021 , 12:33PM Cadila: Gets USFDA approval for Fulvestrant Injection, 250 mg/5 mL (50 mg/mL) per Single-Dose Pre-filled Syringe. Fulvestrant injection is used alone or in combination with other drugs to treat a certain type of breast cancers in woman. The drug would be manufactured at Zydus Biologics, Ahmedabad. The approval is positive as it could strengthen the company’s presence in the Oncology segment in the US.
  • Cadila Healthcare

    22 Jul 2021 , 9:35AM The European Medicines Agency has granted “Orphan Drug Designation” to Saroglitazar Mg for the treatment of patients with Primary Biliary Cholangitis (PBC). Orphan drug status provides companies with a range of incentives, including assistance with trial protocols, reduced regulatory fees, access to a centralized marketing authorization procedure valid in all EU Member States, and a 10-year period of market exclusivity if the treatment eventually is approved. Earlier the USFDA has also granted a Orphan Drug designation and Fast track designation to Saroglitazar. The global market for PBC treatment is expected to grow at a CAGR of 36.3% from 2018 – 2026 and is expected to reach USD 10.8 bn by 2026. Also the company gets USFDA tentative approval for Ibrutinib Tablets, in the strengths of 140 mg, 280 mg, 420 mg and 560 mg. Ibrutinib is used to treat certain type of cancers. The orphan Drug designation for Saroglitazar by European Medicine Agencies and tentative approval for Ibrutinib are positive
  • Cadila Healthcare

    15 Jul 2021 , 11:02AM The company has completed the sale transaction of its Animal Healthcare business effective 14 July 2021. The business transfer agreement for the same was signed on 12 May 2021 and it has been completed within the 90 day window after signing of the definitive agreement
  • Cadila Healthcare

    8 Jul 2021 , 9:17AM Cadila: As per media reports, the Subject Matter Expert Committee of the Indias Drug regulator is expected to take up the company’s application seeking emergency use approval for its three dose Covid Vaccine, in this week. Positive if the Vaccine gets the regulators approval.
  • Cadila Healthcare

    5 Jul 2021 , 10:52AM As per media Viona Pharmaceuticals Inc is recalling 21,240 bottles of metformin hydrochloride extended-release tablets, USP 750 mg in the US, which are manufactured at Cadila’s Facility. The recall is on account of a detection of n-nitrosodimethylamine (NDMA) levels in excess of the acceptable daily intake limit and the Voluntary recall is being classified as a class II recall by the USFDA, hence is unlikely to have any material impact on the financial performance of the company.
  • Cadila Healthcare

    2 Jul 2021 , 2:06PM Cadila: Gets final approval from the USFDA for Emtricitabine and Tenofovir Disoproxil Fumarate Tablets strengths - 100 mg/150 mg, 133 mg/200 mg and 167 mg/250 mg. The drug is used with other HIV medications to help control HIV infection. It helps to decrease the amount of HIV in the patients so that the immune system can work better. The approval is positive and would add to the US sales, which accounts for 43% of Fy21 overall sales.
  • Zydus gets USFDA nod for combination drug use to treat HIV

    2 Jul 2021 , 12:21PM Zydus gets USFDA nod for Emtricitabine and Tenofovir Disoproxil Fumarate tablets
  • Cadila Healthcare

    1 Jul 2021 , 9:34AM Cadila: Has approached the DCGI seeking emergency use authorization for its Vaccine ZyCoV-D, which is the first Plasmid DNA vaccine against Covid. Interim data from the trials demonstrates safety and efficacy levels. Primary efficacy of 66.6% has been attained for symptomatic RT-PCR positive cases in the interim analysis Whereas, no moderate case of COVID-19 disease was observed in the vaccine post administration of the third dose suggesting 100% efficacy for moderate disease. Also the vaccine has been tested on population in the age group 12-18 years and has found to be safe and well tolerated. If the DCGI approves the vaccine it would be positive as the company plans to manufacture 10-12 crore doses of the vaccine annually.
  • Cadila Healthcare

    28 Jun 2021 , 11:27AM As per media reports, the company’s Covid vaccine for children aged 12-18 years is expected to be available by August 2021 end as the trials are likely to be complete by end of July. If the trials are completed in a timely manner and the Vaccine is approved, it could open up a sizeable opportunity as currently there are no vaccines available for age group 12-18 years, hence its potential positive.
  • Cadila Healthcare gets USFDA nod for pemetrexed for injection

    25 Jun 2021 , 11:38AM Zydus Cadila receives tentative approval from USFDA for Pemetrexed for Injection
  • Cadila Healthcare

    24 Jun 2021 , 11:16AM Cadila: Gets tentative approval from the USFDA for Fingolimod Capsules in the strength of .25 mg. Earlier in October 2020 the company received an approval for Fingolimod Capsules in the strength of 0.5mg from the USFDA. The drug is indicated for the treatment of relapsing forms of multiple sclerosis. As of FY2021 the US sales constitute around 43% of overall sales of the company and with the tentative approval Cadila’s offerings in the US markets could be widened and would aid topline growth, hence positive
  • Zydus Cadila receives tentative approval from USFDA for Fingolimod Capsules

    24 Jun 2021 , 11:14AM The group was granted approval to market Fingolimod Capsules in the strength of .5mg. Fingolimod is an immunomodulating drug
  • Cadila Healthcare

    22 Jun 2021 , 9:56AM As per media reports the company has launched new triazole antifungal drug Posaconazole which is effective against fungal diseases and is also recommended as a second line treatment for Mucormycosis. The drug is presently available in the suspension forms and tablets form and the injectable form is under pipeline. Given the rapid increase of Mucormycosis in the second wave of Covid, the drug could have a strong demand and hence positive for Cadila.
  • Cadila Health extends tenure of JV with Bayer Group for 3 years

    21 Jun 2021 , 11:59AM JVA with Bayer (South East Asia) PTE Ltd, one of the companies of the Bayer Group, for a period of three years
  • Cadila Healthcare gets USFDA approval for Brivaracetam tablets

    14 Jun 2021 , 10:46AM Zydus Cadila receives tentative approval from USFDA for Brivaracetam Tablets
  • Cadila Healthcare

    14 Jun 2021 , 10:18AM Cadila: The company has received a tentative approval from the USFDA for Brivaracetam Tablets, in the strengths of 10 mg, 25 mg, 50 mg, 75 mg, and 100 mg. Brivaracetam is used to treat partial-onset of seizures (epilepsy). The tentative approval is positive and will add to the growth in the US business.
  • Cadila Healthcare

    3 Jun 2021 , 12:07PM Cadila: Gets USFDA approval for Osimertinib Tablets in the strengths of 40 mg and 80 mg (US RLD: Tagrisso Tablets). Osimertinib is used to treat lung cancer. It belongs to a class of drugs known as kinase inhibitors. The approval is positive and would add to the US sales growth
  • Zydus Cadila gets tentative nod from USFDA for Osimertinib Tablets

    3 Jun 2021 , 12:02PM Zydus Cadila receives tentative approval from USFDA for Osimertinib Tablets in the strengths of 40 mg and 80 mg
  • Cadila Healthcare gets USFDA nod Fluphenazine Hydrochloride Tablets

    31 May 2021 , 9:52AM Zydus Cadila receives final approval from USFDA for Fluphenazine Hydrochloride Tablets
  • Cadial Healthcare

    31 May 2021 , 9:32AM Cadila: Gets final approval from the USFDA for Fluphenazine Hydrochloride Tablets strengths - 1 mg, 2.5 mg, 5 mg, and 10 mg. This medication is used to treat symptoms of a certain type of mental/mood condition (schizophrenia). The approval is positive for Cadila and would enable grow the US sales. Also the company is planning to test its Covid Vaccine ZyCov-D on children aged 5 years and above. The vaccine is currently undergoing the trials in adults and children aged 12-18 years as well. The management is expecting the emergencu use approval by end of June or July 2021.
  • Cadila Healthcare Limited: Q4FY21 Result Update

    28 May 2021 , 11:02AM Cadila Healthcare Limited: Q4FY21 Result Update - In a growth sweet spot
  • Cadila Healthcare: Q4FY21 – Healthy quarter

    27 May 2021 , 2:55PM Cadila Healthcare: Q4FY21 – Healthy quarter; tax credit leads to adjusted PAT ahead of estimates
  • Cadila Healthcare

    27 May 2021 , 10:22AM Cadila: seeks DCGI approval to undertake clinical trials for monoclonal antibodies cocktail - ZRC-3308 that can neutralize COVID infection. As per the company cocktail of 2 mAbs based products are better equipped to deal with variants than single mAb based products which have a tendency of losing their efficacy with rapidly generating variants. In animal studies ZRC-3308 reduced damage to the lungs in both prophylactic and therapeutic settings and the company s is currently seeking permission to initiate phase 1 of 3 human clinical trials from the DCGI. If it gets the permission and the trials are successfully completed could provide a potential growth opportunities, hence positive. Also the company has tied up with Taiwan based – specialty pharma company TLC to commercialize Liposomal Amphotericin B, a critical drug to treat mucormycosis (black fungus), in India. As per the agreement TLC would manufacture and Supply the drug while Cadila would commercialize it in India. Given the acute shortage of the drug to treat mucormycosis, the demand is likely to be strong hence positive
  • Cadila Healthcare seeks nod to undertake trials for antibodies cocktail

    27 May 2021 , 10:16AM Zydus seeks DCGI approval to undertake clinical trials for monoclonal antibodies cocktail that can neutralise COVID infection
  • Zydus and TLC sign agreement to market Liposomal Amphotericin B

    26 May 2021 , 1:11PM Zydus, TLC sign agreement to market Liposomal Amphotericin B, a critical drug to treat Black Fungus or Mucormycosis in India
  • Cadila Healthcare

    25 May 2021 , 9:08AM Cadila: The company is looking to triple the monthly production of COVID-19 vaccine candidate – ZyCoV-D to as many as 30 million doses in around the next 4-5 months from 10 mn dosses per month now. Also the management has stated that it plans to submit the Vaccine for emergency use authorization to the regulator in May 2021 month as the vaccine is currently undergoing late-stage trials in nearly 30,000 adults. Expansion of the vaccine manufacturing capacity would be done through in house as well as third party manufacturers. Capacity expansion for the vaccine is positive for the company subject to the receipt of regulatory approvals
  • Cadila Healthcare

    24 May 2021 , 9:13AM Cadila: Launched Trastuzumab Emtansine, the first Antibody Drug Conjugate (ADC) biosimilar and a highly effective drug for treating both Early and Advanced HER2 positive Breast Cancer cancers in India. The product would be launched under the brand “Ujvira” and would be available in two strengths – 100mg and 160 mg. Cadila has priced the drug at Rs 32,495 and can significantly reduce the treatment cost by around 80%. The product launch is positive and would add to the India sales which accounts for around 40% of overall sales.
  • Cadila Healthcare

    12 May 2021 , 11:33AM Zydus Animal Health and Investment Limited (ZAHL) a wholly owned subsidiary of Cadila has entered in to a business transfer agreement for disposal of its Animal Healthcare Established Markets Undertaking to Zenex Animal Health India Private Limited (Zenex) by way of slump sale subject to certain closing date adjustments specified in the agreements. The turnover of the undertaking for FY20 stood at Rs 513 cr representing 4% of the consolidated revenues of the company and EBITDA stood at RS 87.6 Cr (3% of the consolidated EBITDA). The net worth of the said undertaking at Rs 2203.6 Cr, is around 21% of the total net worth of the Company. The estimated consideration for the transaction is Rs 2921 cr.
  • Cadila Healthcare to sell animal healthcare biz

    12 May 2021 , 11:31AM Zydus Cadila entity to sell its India focused Animal Health Business to Multiples Alternate Asset Management led consortium
  • Cadila Healthcare

    11 May 2021 , 3:02PM Cadila Halthcare: Recently the company had received emergency use approval for Virafin, (injection) which as per the company cuts the oxygen support needed for Covid positive patient. Cadila has now fixed the price of Virafin at Rs 11,995 per dose and has also started dispatches. Given the surge in the Covid cases in India, the demand for Virafin is expected to be strong.
  • Cadila Healthcare

    5 May 2021 , 2:11PM Bayer PTE Limited (South East Asia) and Cadila Health care had entered in to a partnership agreement dated 28 January 2011 for carrying on business of marketing of pharmaceutical products. Further to this Cadila has announced today that it has signed another agreement to extend the existing agreement by two months more to explore possibilities of further Collaboration. Further details on this are awaited
  • Cadila extend joint venture Tenure with Bayer

    5 May 2021 , 12:15PM Cadila Healthcare signs an agreement to extend the tenure of the joint venture agreement with Bayer
  • Cadila Healthcare

    5 May 2021 , 10:32AM As per media reports, Cadila is expecting the first set of its interim efficacy data for its covid-19 vaccine this month – May 2021, following which the company could immediately apply for an emergency use authorization for the Vaccine with the Indian drug regulator. The company has started the phase III trial of its vaccine in February 2021 with 28000 participants. Positive if the interim trial data is encouraging and basis this the company gets the regulators’ approval.
  • Zydus get DCGI nod for emergency use of Pegylated Interferon alpha-2b

    23 Apr 2021 , 3:35PM Zydus receives emergency use approval from Indian regulator (DCGI) for the use of Pegylated Interferon alpha-2b, 'Virafin' in treating moderate COVID-19 infection in adults
  • Cadila Healthcare

    23 Apr 2021 , 11:48AM Cadila: Gets USFDA approval for Propafenone Hydrochloride ExtendedRelease Capsules USP, strength - 225 mg, 325 mg, and 425 mg. Propafenone is an anti-arrhythmic drug and works by blocking the activity of certain electrical signals in the heart that can cause an irregular heartbeat. The approval is positive as it would add to the US business growth, which is ~45% of the overall FY2020 revenues.
  • Zydus Cadila receives final approval from USFDA for Propafenone Hydrochloride Extended-Release Capsules

    23 Apr 2021 , 11:36AM It works by blocking the activity of certain electrical signals in the heart that can cause an irregular heartbeat.
  • Cadila Healthcare

    20 Apr 2021 , 10:44AM As per media reports, Astrazeneca AB has filed a complaint in the Delaware Federal Court to block Zydus Cadila’s proposed generic version of its lung Cancer drug Tagrisso, which infringes one of its patients. Astrazeneca has asked the court to block Zydus Cadila from making or selling the proposed generic until its patent expires in 2035. This is unlikely to have any material impact on the financial performance of the company.
  • Stock Update – Cadila Healthcare

    20 Apr 2021 , 10:18AM Stock Update – Cadila Healthcare Limited: In a sweet spot for sturdy growth
  • Cadila Healthcare

    13 Apr 2021 , 9:35AM The company has approached DCGI seeking approval for its Covid Vaccine candidate - Pegylated Interferon Alpha 2b (PegiHep). The interim results of phase III trials shows better efficacy levels and could help patients recover faster, avoiding much of the complications seen in the advanced stages of the disease. Around 91.15% of patients treated with PegiHep were RT PCR negative by day 7 as compared to 78.90% on the standard of care (SOC) arm. If the Vaccine is approved by DCGI, could be positive for Cadila given the strong demand due to surging covid cases.
  • Cipla, Cadila

    12 Apr 2021 , 10:44AM Considering the surge in the Covid cases across the country, the Government has restricted the exports of Remdesivir injection and Remdesivir API. Also basis the surge in Covid cases companies are ramping up production of Remdesivir so as to be able to cater to the increasing domestic demand.
  • Zydus Cadila gets final nod from USFDA to market Ibrutinib Capsules

    8 Apr 2021 , 1:38PM Zydus Cadila announces USFDA approval for First Generic for Ibrutinib Capsules, 70 mg and gets eligibility for 180-day exclusivity
  • Cadila Healthcare

    8 Apr 2021 , 10:08AM Gets final approval from the USFDA for Ibrutinib Capsules strength - 70 mg and 140 mg. Ibrutinib is used to treat certain cancers, such as mantle cell lymphoma, chronic lymphocytic leukemia/small lymphocytic lymphoma, and Waldenstrom's macroglobulinemia. The company is a first one to get approval for generic Ibrutinib and also gets a 180 day of generic drug exclusivity for Ibrutinib. Given the 180 day exclusivity for the drug, the approval is positive.
  • Zydus seeks DCGI approval for the use of Pegylated Interferon alpha-2b in treating COVID-19

    5 Apr 2021 , 9:43AM Company applies for an Additional Indication with the DCGI for the use of PegIFN in the treatment of COVID 19
  • Cadila Healthcare

    25 Mar 2021 , 1:55PM Cadila: has received tentative approval from the USFDA for Emtricitabine and Tenofovir Disoproxil Fumarate Tablets strength - 100 mg/150 mg, 133 mg/200 mg and 167 mg/250 mg. These tablets are used with other HIV medication to help control HIV infection and are a combination of two drugs Emtricitabine and Tenofovir Disoproxil Fumarate, which helps to decrease the amount of HIV in the body so that the immune system can work better. The approval is positive as it would help grow the US sales, which constitute around 45% of overall FY20 sales.
  • Zydus Cadila gets USFDA nod for Emtricitabine & Tenofovir Disoproxil Fumarate tablets

    25 Mar 2021 , 1:34PM Emtricitabine and Tenofovir Disoproxil Fumarate Tablets are used with other HIV medications to help control HIV infection
  • Cadila Healthcare

    25 Mar 2021 , 10:50AM The company has significantly reduced the prices of its generic version of Remdesivir, which is branded as Remdac. The company has reduced the prices to RS 899 per 100 mg vial as against the launch price of RS 2800 per 100 mg vial. With the onset of the vaccines the demand for Remdesivir has reduced and hence the reduction in prices is unlikely to have any material impact on the financial performance of the company
  • Zydus announces settlement of patent litigation in US

    24 Mar 2021 , 12:06PM Zydus announces settlement of patent litigation for Generic of Revlimid in the US
  • Cadila Healthcare

    9 Mar 2021 , 10:24AM Cadila: As per media news, the company is likely to release the phase III data for Covid -19 Vaccine ZyCov-D by the end of March or early April 2021. The Phase III trials of the vaccine were done on around 30,000 people across 60 locations and the company aims to supply around 100 to 150 mn doses of its vaccine in CY2021. Positive, If the trials are successful and the Vaccine is approved by regulatory authorities.
  • Cadila Healthcare

    9 Mar 2021 , 9:31AM As per media reports, Multiples Alternate Asset Management and Canadian pension fund giant CPPIB have teamed up to emerge as the lead contenders to acquire company’s animal healthcare business. The move is a part of the strategic initiative by Cadila to prune its diversified portfolio so that it can focus on few select business for growth. As of FY2020 the animal health business contributed ~4% of the overall revenues of the company. The deal is likely to be valued around Rs 2500 to Rs 3000 crore. Positive if the deal goes through.
  • Cadila Healthcare

    25 Feb 2021 , 1:38PM Cadila Healthcare: Gets final approval from the USFDA for Nortriptyline Hydrochloride Capsules USP, Strength - 10 mg, 25 mg, 50 mg and 75 mg. The drug is used to treat mental/mood problems such as depression. It may help improve mood and feelings of well-being, relieve anxiety and tension, and increase one’s energy level. The approval is positive as it would strengthen the US product portfolio.
  • Zydus Cadila gets nod from USFDA for Nortriptyline Hydrochloride Capsules

    25 Feb 2021 , 12:15PM Cadila Health gets USFDA nod for Nortriptyline Hydrochloride Capsules, used for treatment of depression
  • Cadila Healthcare

    25 Feb 2021 , 10:21AM Cadila Healthcare: a wholly owned step down subsidiary company of Zydus group - Sentynl Therapeutics Inc and Cyprium Therapeutics (a Fortress Biotech Partner Company) have entered in to an asset purchase agreement to commit development funding for and acquire Cyprium’s proprietary rights to CUTX-101, its Copper Histidinate product candidate, for treatment of Menkes disease. Sentynl has acquired CUTX-101, for $20 million in upfront and regulatory milestone payments through NDA approval, as well as potential sales milestones plus royalty payments. As per the terms of the agreement Cyprium would retain 100% ownership over any USFDA priority review voucher that may be issued at NDA approval for the product. The development is positive for Cadila as it could strengthen the product pipeline, if the product gets regulatory approval
  • Cadila Healthcare

    19 Feb 2021 , 12:12PM Cadila: Gets final approval from the USFDA to market Droxidopa Capsules in strength of 100 mg, 200 mg, and 300 mg. The drug is used to treat low blood pressure that causes severe dizziness or a lightheaded feeling. It is indicated for use in people with conditions of the nervous system that can cause low blood pressure. The approval is positive as it would add to the US sales, which account for around 45% of FY2020 sales.
  • Zydus Cadila receives final approval from USFDA for Droxidopa Capsules

    19 Feb 2021 , 12:08PM Droxidopa Capsules, used to treat low blood pressure that causes severe dizziness or a lightheaded feeling
  • Cadila Healthcare

    18 Feb 2021 , 9:10AM As per media news, Pfizer has alleged that Zydus’s proposed generic version of Xeljanz XR in 22-mg tablet form infringes two patents on its blockbuster ulcerative colitis drug. Pfizer is seeking court order to block Zydus from going ahead with proposed generic version of Xeljanz XR. As per the USFDA the patents for the drug would expire in March 2023 and December 2025. This is negative as it could delay the product launch by Cadila.
  • Cadila Healthcare: Q3FY21

    5 Feb 2021 , 3:06PM Cadila Healthcare: Q3FY21 – Healthy performance; PAT marginally missed estimates
  • Zydus completes Phase-I trials of its single dose

    4 Feb 2021 , 10:56AM Cadila's Zydus announces completion of Phase-I trials of ZY19489 A single dose cure for Malaria in collaboration with MMV
  • Cadila Healthcare

    28 Jan 2021 , 2:48PM The USFDA has granted ‘Orphan Drug Designation’ to Saroglitazar Mg for the treatment of patients with Primary Biliary Cholangitis (PBC). Orphan drug designation provides eligibility for certain development incentives, including tax credits for qualified clinical testing, prescription drug user fee exemptions and seven-year marketing exclusivity post FDA approval. This follows the grant of ‘Fast Track Designation’ by the USFDA to Saroglitazar Mg for in December 2020. The company earlier has completed a phase II study for Saroglitazar. The treatment options are still evolving for PBC and Saroglitazar holds immense potential based on its safety and efficacy profile so far. As per coherent Market insights the market for PBC treatment is expected to grow at a CAGR of 36.3% from 2018 — 2026 and is expected to reach USD 10.8 bn by 2026. Given the award of Orphan Drug Designation and earlier award of Fast Track Designation, points at need to address this serious health condition which is an unmet medical need. This would be positive if the drug completes the studies successfully and gets regulatory approval.
  • Cadila's Zydus grant Orphan Drug Designation by the USFDA

    28 Jan 2021 , 10:45AM Cadila's Zydus granted Orphan Drug Designation by the USFDA for Saroglitazar in the treatment of patients with Primary Biliary Cholangitis
  • Cadila Healthcare

    25 Jan 2021 , 10:06AM Cadila: Gets final approval from the USFDA for Liothyronine Sodium Tablets USP, 5 mcg, 25 mcg, and 50 mcg. Liothyronine is a man-made form of thyroid hormone which is used to treat an underactive thyroid (hypothyroidism). The US sales for the company constitute around 45% of the total and this approval is positive as it could add to the growth of the US topline.
  • Cadila Healthcare

    25 Jan 2021 , 9:14AM Cadila has received final approval from the USFDA to market Liothyronine Sodium Tablets, used to treat an underactive thyroid
  • Cadila Healthcare

    13 Jan 2021 , 10:30AM Covid Vaccine candidate – ZyCov-D has demonstrated promising results in the first and second phase of clinical trials and has enrolled 30,000 volunteers for Phase III trials.. Further the company has said that it would be able to achieve the targeted supply of 100-150 million doses by the end of 2021. Once approved, would be positive as it would open substantial growth opportunities.
  • Cadila Healthcare

    4 Jan 2021 , 11:04AM Gets Drug Controller General of India’s permission to commence phase III clinical trials for its Covid 19 Vaccine – Zycov –D. The trial would be initiated with a 30,000 volunteers. Positive, if the trials are successfully completed and the vaccine is approved by the regulator.
  • DGCI nods Cadila’s Saroglitazar Mg

    30 Dec 2020 , 10:49AM Drug used to treat liver disease; contributed ~27% of FY20 sales
  • Cadila Healthcare

    7 Dec 2020 , 2:06PM Has received permission to commence the phase I trial of ZYIL1, a novel oral small molecule NLRP3 inhibitor candidate. NLRP3 inflammasomes are involved in the inflammation process by production and release of proinflammatory cytokines. This could result in the onset and development of various kinds of diseases in the body. If the trials are successfully completed and the drug approved could be a positive as it could boost the topline.
  • Zydus gets permission to initiate the Phase 1 trial of ZYIL1

    7 Dec 2020 , 12:20PM Zydus announces Phase I trials of ZYIL1, a novel oral small molecule NLRP3 inflammasome inhibitor
  • Cadila Healthcare

    4 Dec 2020 , 12:05PM Cadila: The company has received an approval from the Drugs Controller General of India (DCGI) to start the Phase 3 clinical trial in CoVID-19 patients with its biological therapy, Pegylated Interferon alpha-2b – “PegiHepTM”. The trials which will commence in the month of December 2020 will be conducted on 250 patients across 20-25 centres in India. If the trials are successfully completed and the drug is approved, it would be positive as the demand for the drug would surge substantially. Also Cadila is working with USFDA to open an Investigational New drug Application (NDA) so as to initiate appropriate clinical trials in the US.
  • Zydus gets DCGI nod to start phase-3 clinical trials in COVID patients with PegiHep

    4 Dec 2020 , 11:56AM Zydus receives approval from DCGI to commence Phase III clinical trials with Pegylated Interferon alpha-2b in India
  • Cadila Healthcare

    9 Nov 2020 , 11:26AM As per media news, the company has completed the dosing of its Covid Vaccine on 1000 patients in the phase II of the trials and looks to submit the data to the regulator this month. Further it is expected to test its Covid vaccine candidate, on about 30,000 people in the Phase-3 trials that it plans to start next month. The results of the phase III trials are expected to come out by March – April 2021. If the trials are successful and the vaccine is approved, it would open up substantial growth potential Vacci
  • Cadila Healthcare Limited: Q2FY2021 Result Update

    4 Nov 2020 , 11:09AM Cadila Healthcare Limited: Q2FY2021 Result Update - Strong Quarter; Sturdy growth outlook
  • Cadila Healthcare

    29 Oct 2020 , 1:59PM Cadila: Gets tentative approval from the USFDA for Linagliptin Tablets, 5 mg. Linagliptin is a dipeptidyl peptidase-4 (DPP-4) inhibitor indicated as an adjunct to diet and exercise to improve glycemic control in adults with Type 2 diabetes. The approval is positive as it would enable to widen the product offerings in the US market
  • Zydus Cadila receives tentative approval from USFDA for Linagliptin Tablets

    29 Oct 2020 , 11:49AM It's a dipeptidyl peptidase-4 inhibitor indicate as an adjunct to diet and exercise to improve glycemic control in adults with Type 2 diabetes mellitus
  • Cadila Healthcare

    27 Oct 2020 , 11:16AM As per media reports, the company is in talks with potential partners to ramp up production capacity of its Vaccine candidate if it passes Human clinical trials. The company is looking to hire contract manufacturers for an additional 50 million to 70 million doses of its vaccine, in addition to 100 million that will come from Cadila’s own capacity.
  • Zydus Cadila gets final nod from USFDA for Albuterol Tablets

    23 Oct 2020 , 11:45AM Zydus Cadila receives final approval from USFDA for Albuterol Tablets, used to open up medium, large airways in lungs
  • Cadila Healthcare

    20 Oct 2020 , 12:31PM Gets final approval from the USFDA for Solifenacin Succinate Tablets in the strengths of 5 mg and 10 mg. Solifenacin Succinate is a symptomatic treatment of urge incontinence and/or increased urinary frequency and urgency as may occur in patients with overactive bladder syndrome. The approval is positive and would help grow the US business sales
  • Zydus Cadila gets USFDA nod for Solifenacin Succinate tablets

    20 Oct 2020 , 10:13AM Cadila Health's Zydus gets USFDA nod for a drug used to treat overactive bladders
  • Cadila Healthcare

    19 Oct 2020 , 9:57AM Cadila: Gets USFDA final approval for Ursodiol Capsules USP - 300 mg. Ursodiol is in a class of medications called gallstone dissolution agents. It is used to treat people with primary biliary cirrhosis, which is a type of liver disease. Also Cadila has got tentative approval for Linagliptin and Metformin Hydrochloride Tablets Strength - 2.5 mg/500 mg, 2.5 mg/850 mg, and 2.5 mg/1,000 mg, used to treat patients with type 2 diabetes. The US revenues constitute around 45% of FY2020 sales and receipt of the product approvals is positive as it would drive the US sales growth.
  • Cadila gets final nod for cholesterol drug

    19 Oct 2020 , 9:41AM Zydus Cadila gets USFDA nod for Ursodiol Capsules and Tentative Approval for Linagliptin and Metformin Hydrochloride Tablets
  • Cadila Healthcare

    16 Oct 2020 , 11:40AM Cadila: gets final approval from the USFDA for Fingolimod Capsules, 0.5 mg. Fingolimod is an immune-modulating drug. It is a sphingosine 1-phosphate receptor modulator indicated for the treatment of relapsing forms of multiple sclerosis. Fingolimod is an immunomodulating drug indicated for the treatment of relapsing forms of multiple sclerosis. Cadila has also received the final approval from the USFDA for Verapamil Hydrochloride Injection USP, 5 mg/2 mL (2.5 mg/mL) and 10 mg/4 mL (2.5 mg/mL), Single-Dose Vials. Verapamil injection is used to rapidly or temporarily restore normal heartbeats in people with certain heart rhythm disorders. Both the product approvals are positive as they would fuel the revenue growth in the US business
  • Zydus gets final nod from USFDA to market Fingolimod Capsules

    16 Oct 2020 , 10:29AM Zydus Cadila receives final approval from USFDA for Fingolimod Capsules and Verapamil Hydrochloride Injection
  • Cadila Healthcare

    8 Oct 2020 , 12:06PM Cadila: announced that it is launching Forglyn pMDI, India’s first pressurized Metered Dose Inhaler (pMDI) with a combination of Long Acting Muscarinic Antagonist (LAMA) and Long Acting Beta Agonist (LABA) for patients suffering from Chronic Obstructive Pulmonary Disease in India. The medicine is developed using the company’s in house innovation formulations technology and is priced at Rs 495 per pack. This is a positive and will help grow the domestic formulations business which accounts for ~27% of FY20 sales.
  • Cadila Healthcare launches pressurized Metered Dose Inhaler for patients

    8 Oct 2020 , 11:10AM Zydus launches India's first pressurized Metered Dose Inhaler for patients suffering from Chronic Obstructive Pulmonary Disease
  • Cadila Healthcare

    5 Oct 2020 , 10:24AM As per media reports, Zydus healthcare has launched generic anti-diabetic drug - Dapagliflozin tablets across India under the brand name 'Dapaglyn' at highly affordable price to increase patient access. The medicine has been launched in the strengths of 10mg and 5mg priced at Rs 17 and Rs 14 respectively. The pricing compares as 1/3rd the price of existing medicines available. This is positive as it would help grow the Indian formulations revenues.
  • Cadila Healthcare

    25 Sep 2020 , 12:07PM Gets Final approval from the USFDA for Dimethyl Fumarate DelayedRelease Capsules in the strengths of 120 mg and 240 mg. Cadila Is eligible for 180 days of generic drug exclusivity for the drug. The drug is indicated for the treatment of patients with relapsing forms of multiple sclerosis. The approval is positive as it could help grow US revenues for the company.
  • Zydus Cadila receives final nod from USFDA

    25 Sep 2020 , 11:07AM Zydus Cadila gets USFDA nod for anti-Inflammatory drug Dimethyl Fumarate Delayed-Release capsules
  • Cadila Healthcare

    24 Sep 2020 , 11:42AM Gets approval from the USFDA for Palbociclib Capsules in the strengths of 75 mg, 100 mg, and 125 mg. Palbociclib is an anti-cancer medicine that interferes with the growth and spread of cancer cells in the body. The approval is positive for the company and will help to grow the US business.
  • Zydus Cadila receives tentative approval from USFDA

    24 Sep 2020 , 10:21AM Zydus Cadila receives tentative approval from USFDA for Palbociclib Capsules
  • Zydus Cadila receives tentative approval from USFDA

    24 Sep 2020 , 10:19AM Zydus Cadila receives tentative approval from USFDA for Palbociclib Capsules
  • Zydus Cadila receives tentative approval from USFDA

    24 Sep 2020 , 10:18AM Zydus Cadila receives tentative approval from USFDA for Palbociclib Capsules
  • Cadila Healthcare

    18 Sep 2020 , 4:18PM Gets USFDA approval for Potassium Chloride Extended Release Tablets in the strengths of 10 mEq (750 mg) and 20 mEq (1500 mg). The medication is a mineral supplement used to treat or prevent low amounts of potassium in the blood. The Reference listed drug is K-Dur Extended Release tablets – The approval is positive as it would add to the sales of the US business
  • Zydus Cadila gets nod from USFDA to market Extended Release tablets

    18 Sep 2020 , 11:47AM Zydus Cadila receives final approval from USFDA for Potassium Chloride Extended-Release Tablets
  • Buzzing in trade: Pharma stocks

    18 Sep 2020 , 10:59AM Pharma stocks trade higher
  • Cadila Healthcare

    11 Sep 2020 , 2:54PM Received final approval from the USFDA for Doxorubicin Hydrochloride Liposome Injection (US RLD: Doxil Liposome Injection) in the strengths of 20 mg/10 mL (2 mg/mL) and 50 mg/25 mL (2 mg/mL) Single-Dose Vials. This is the group’s first approval for a complex injectable which has been developed in-house. U.S. sales for Liposomal Doxorubicin Injection were approximately $124 million for the 12 months ending July 2020, according to IQVIA. The approval is positive as it would add to the US sales growth
  • Cadila Healthcare

    9 Sep 2020 , 2:08PM Gets approval from USFDA to Empagliflozin and Linagliptin Tablets (US reference listed drug: Glyxambi Tablets) in the strengths of 10 mg/5 mg and 25 mg/5 mg. This medication contains a combination of Empagliflozin and Linagliptin. Empagliflozin and Linagliptin are oral diabetes medicines that help control blood sugar levels. The medicine is used to treat type 2 diabetes mellitus. The approval is positive as it would help grow the US revenues for the company
  • Zydus Cadila receives tentative approval from USFDA

    9 Sep 2020 , 1:04PM Zydus Cadila receives tentative approval from USFDA for Empagliflozin and Linagliptin Tablets
  • Zydus Cadila receives final nod from USFDA

    3 Sep 2020 , 11:16AM Zydus Cadila receives final approval from the USFDA to market Midodrine Hydrochloride Tablets
  • Cadila Healthcare

    2 Sep 2020 , 10:41AM Gets approval from the USFDA to market Cisatracurium Besylate Injection USP in the strength of 20 mg (base)/10 mL (2 mg/mL) Multiple-Dose Vial. Cisatracurium Besylate is a non-depolarizing skeletal neuromuscular blocker for intravenous administration and provide skeletal muscle relaxation in adults during surgical procedures or during mechanical ventilation in the ICU. The drug would be made at the company’s Liva plant. The approval is positive at it would aid growth in the US business.
  • Zydus gets USFDA nod for Cisatracurium Besylate injection

    2 Sep 2020 , 10:36AM Zydus gets US FDA nod for Cisatracurium Besylate injection which is used to maintain neuromuscular relaxation in surgery
  • Cadila Healthcare

    13 Aug 2020 , 4:00PM Cadila: Received final approval from the USFDA to market Sevelamer Carbonate Tablets (US RLD - Renvela Tablets) in the strength of 800 mg. The drug is a phosphate binder and is used to control phosphorus levels in people with chronic kidney disease who are on dialysis. The Drug will be manufactured at the company’s Ahmedabad SEZ facility. The approval is positive as it would aid the US business growth
  • Cadila Healthcare

    13 Aug 2020 , 11:38AM Cadila: launches Remdesivir under the brand name Remdac. The drug is priced at Rs 2800 for a 100 mg lyophilized injection. Remdac is the most economical Remdesivir brand in India to treat Covid patients. The drug would be made available through India through the groups strong distribution network. The launch is positive in the light of increasing Covid patients across the country
  • Zydus introduces Remdac for COVID treatment

    13 Aug 2020 , 10:09AM Zydus launches RemdacTM (Remdesivir) for the treatment of COVID 19 in India
  • Cadila Healthcare

    11 Aug 2020 , 11:25AM As per media reports, the company has stated that it will be submitting the data and outcomes for its studies for Covid vaccine to the regulator. If the outcome is favourable the company is hopeful of making the vaccine available in the market by March 2021.
  • Cadila Healthcare

    6 Aug 2020 , 11:43AM Cadila Healthcare Limited: Q1FY21 result update - Healthy Quarter; still in a gearing up stage
  • Cadila Healthcare

    5 Aug 2020 , 3:10PM Cadila Healthcare: Q1FY21 – Healthy performance; results better than estimates
  • Cadila Healthcare

    5 Aug 2020 , 10:21AM The company has completed the phase 1 of clinical trials of its Covid 19 vaccine candidate and have now begun the Phase II of the studies. Completion of Clinical trials is positive.
  • Cadila Healthcare gets USFDA tentative nod to market Parkinsons disease drug

    3 Aug 2020 , 2:08PM Zydus Cadila receives tentative approval from the USFDA for Carbidopa and Levodopa Extended-Release Capsules
  • Cadila Healthcare

    3 Aug 2020 , 11:54AM The company is positive about its growth momentum in the United States driven by new product launches and expansion in overall product offerings. In the annual report the company is planning to introduce additional "topical, transdermal and injectable products in the US along with other new launches. US contributed around 45% of the consolidated revenues and the growth momentum is likely to continue backed by new product launches and expansion of overall product offerings
  • Cadila Healthcare

    3 Aug 2020 , 9:46AM Gets tentative approval from the USFDA to market Carbidopa and Levodopa Extended-Release Capsules with strength - 23.75 mg/95 mg, 36.25 mg/145 mg, 48.75 mg/195 mg, and 61.25 mg/245 mg. This medication is used to treat the symptoms of Parkinson›s disease or Parkinsons like conditions. The approval is positive for the company, it would add to the growth of the US business.
  • Cadila Healthcare

    27 Jul 2020 , 11:46AM Cadila: disclosed impact of COVID-19 on business operations. The key highlights are as follows
  • Cadila Healthcare

    23 Jul 2020 , 11:19AM The company has received approval from the USFDA, to initiate clinical trials of Desidustat in Chemotherapy Induced Anemia (CIA). Cancer Patients undergoing chemotherapy develop anemia. Desidustat has been specifically designed to improve haemoglobin, reduce hepcidin and thereby treat anemia. The receipt of the approval is positive as, if the trials are successful it could offer potential growth opportunities
  • Zydus gets USFDA nod to initiate clinical trials

    23 Jul 2020 , 9:56AM Zydus gets USFDA nod to initiate clinical trials of Desidustat in cancer patients receiving chemotherapy
  • Cadila Healthcare

    20 Jul 2020 , 10:04AM Gets final approval from the USFDA to market Butalbital, Acetaminophen and Caffeine Tablets in the strengths 50mg/325mg/40 meg. This combination of medication is used to treat symptom of complex tension (or muscle contraction), headache. The drug will be manufactured at Nesher Pharma’s manufacturing facility at St. Louis, USA. The approval is positive as it could to the US business growth.
  • Cadila Healthcare

    17 Jul 2020 , 10:58AM Gets USFDA Approval for Betamethasone Dipropionate ointment. The ointment is used for treating itching & skin conditions such as Eczema. The approval is positive as it would help improve the US business revenues.
  • Zydus receives approval from Mexican regulatory authority. Stock up

    17 Jul 2020 , 10:57AM Zydus receives approval from COFEPRIS to conduct clinical trials in Mexico with Pegylated Interferon alpha-2b to treat novel Coronavirus
  • Cadila Healthcare

    16 Jul 2020 , 12:52PM Gets USFDA approval for its supplemental Abbreviated New Drug Application (SANDA) for Doxycycline Injection USP, 100 mg/Vial. The product will be manufactured at Cadila Healthcare Ltd’s injectable facility at Jarod, Vadodara. The approval is positive as it would add to the US business revenues.
  • Zydus get sANDA approval from the USFDA

    16 Jul 2020 , 11:47AM Zydus' receives sANDA approval from the USFDA for manufacturing of Doxycycline Injection at Jarod, Vadodara
  • Cadila Healthcare

    15 Jul 2020 , 2:01PM Gets USFDA approval for Betamethasone Dipropionate Ointment USP 0.05%. Ointment is used to treat a variety of skin conditions - eczema, dermatitis, allergies, rash. The ointment will be manufactured at the Ahmedabad plant. The approval is positive as it would enable to improve the US sales of the company
  • Zydus Cadila receives final approval from USFDA for Betamethasone Dipropionate Ointment

    15 Jul 2020 , 1:59PM Betamethasone Dipropionate Ointment is used to treat a variety of skin conditions
  • Cadila Healthcare Ltd

    15 Jul 2020 , 10:32AM Announced that the Adaptive Phase I/ II human clinical trials of its vaccine, ZyCoV-D (for treating Covid-19) commenced today with the first human dosing. The Study will be enrolling around 1000 subjects and will assess the safety, tolerability and immunogenicity of the vaccine. The commencement of human trials marks key milestone since launching of the accelerated vaccine development program in Feb 2020. Positive, if the trials are successful and the vaccine is approved as it would result in a surge in demand for the vaccine given the increasing Covid 19 cases.
  • Zydus starts human dosing of its vaccine 'ZyCov-D'

    15 Jul 2020 , 9:31AM Zydus starts the Human Dosing for Adaptive Phase I &II clinical trials'
  • Cadila Healthcare

    6 Jul 2020 , 11:59AM Cadila: received approval from the regulatory authority of Mexico, COFEPRIS, for its one of its lead research candidate Desidustat to be tested in the management of COVID-19. The company will be conducting a Phase 2b, Multicenter, Open-label, Randomized, Comparator- Controlled Study to Evaluate the Efficacy and Safety of Desidustat Tablet for the management of COVID-19 patients. The drug is under trial stage and would be positive if the trials are successfully completed and the drug is approved for Covid 19 treatment.
  • Zydus gets DCGI nod for human clinical trials

    3 Jul 2020 , 11:18AM Zydus Cadila gets DCGI approval for human clinical trials of COVID-19 vaccine
  • Cadila Healthcare

    3 Jul 2020 , 10:10AM Announced that its vaccine candidate for COVID-19 (ZyCoV-D) developed indigenously by the company has successfully completed the preclinical phase. It has received permission from the Drug Controller General of India - Central Drugs Standard Control Organisation to initiate Phase I/II human clinical trials in India. The company has already manufactured clinical GMP batches of the vaccine candidate and plans to initiate the clinical trials in July 2020 across multiple sites in India in over 1000 subjects. The outcome of the clinical trial would be awaited and is key point to watch. If approved, would be positive as it could substantially drive the revenues.
  • Cadila Healthcare

    24 Jun 2020 , 1:36PM Gets final approval from USFDA to market Meclizine Hydrochloride Tablets in strengths of 12.5 mg and 25 mg. Meclizine is an antihistamine that is used to prevent and treat nausea, vomiting, and dizziness caused by motion sickness. It is also used to reduce dizziness and loss of balance (vertigo) caused by inner ear problems. The drug will be manufactured at SEZ facility, Ahmedabad. Cadila’s US business accounts for ~45% of the sales and the approval could add to the US business growth.
  • Cadila Healthcare gets final nod from USFDA

    24 Jun 2020 , 11:53AM Zydus receives final approval from the USFDA for Meclizine Hydrochloride Tablets
  • Cadila Healthcare

    22 Jun 2020 , 12:02PM Cadila Healthcare: Q4FY2020 Result update - Uncertainties to stay; retain hold
  • Cadila Healthcare

    19 Jun 2020 , 3:20PM Cadila Healthcare: Q4FY20 Mixed performance
  • IPCA, CADILA

    19 Jun 2020 , 12:43PM The Government of India has lifted the ban on the export of Hydroxychloroquine for both API and formulations with immediate effect. On March 25,2020 the drug export was banned to ensure the availability to treat patients for Covid-19. Though during the ban India has supplied the medicines to over 120 countries and so lifting of the ban is unlikely have any material benefit.
  • Cadila Healthcare

    16 Jun 2020 , 11:34AM Gets final approval from USFDA to market Deferasirox Tablets in strength of – 90 mg, 180mg and 360 mg. The medicine is used to treat iron overload caused by blood transfusions or genetic blood disorder in adults and children. The drug will be made at the company’s SEZ plant in Ahmedabad. Positive as this would help to improve the US business.
  • Zydus Cadila

    15 Jun 2020 , 12:21PM Zydus Cadila has signed a non-exclusive licensing agreement with Gilead Sciences Inc for manufacturing of API and Finished Product for Remdesivir, which has been granted emergency use authorizations for treatment against Covid -19
  • IPCA, Cadila

    10 Jun 2020 , 11:40AM As per media reports, India is considering lifting the ban on export of hydroxychloroquine (HCQ) used in the treatment of Covid-19. The DGFT (Directorate general of Foreign trade) in its order dated 4th April 2020 had mentioned that the export of HCQ is banned without any exception. However afer the US claimed it to be effective medicine against Covid-19 patients, the demand surged. Since April, India has been exporting HCQ on a case-by-case basis to the US as well as to other countries as well. The lifting of the export ban is unlikely to have any material impact on these companies as the exports were happening on a selective basis.
  • Cadila Healthcare

    5 Jun 2020 , 2:14PM Gets Final approval from the USFDA to market Atazanavir Capsules (US RLD: Reyataz Capsules) in the strengths of 150mg, 200 mg and 300 mg. Drug is used to treat infection of the Human Immunodeficiency Virus (HIV). It is used in combination with other antiretroviral drugs to treat HIV-1 infection. The drug would be manufactured at the Ahmedabad Sez plant. The approval could help improve the US business of Cadila.
  • Cadila get USFDA nod to market Atazanavir Capsules

    5 Jun 2020 , 12:45PM Zydus Cadila receives final approval from USFDA for Atazanavir Capsules
  • Cadila Healthcare

    29 May 2020 , 9:51AM The Baddi manufacturing facility has received an Establishment Inspection report (EIR) from the USFDA and the classification of the facility is No Action Indicated (NAI). The receipt of the EIR indicates successful closure of the inspection, so Positive
  • Cadila Healthcare

    18 May 2020 , 10:50AM Received tentative approval from the USFDA to market Droxidopa Capsules - in the strengths of 100 mg, 200 mg, and 300 mg. Droxidopa can lessen symptoms of low blood pressure when standing (orthostatic hypotension), such as dizziness and light-headedness. The drug will be manufactured at the group’s manufacturing facility at SEZ, Ahmedabad. Positive as the approval would strengthen the US business.
  • Cadila Healthcare Ltd

    11 May 2020 , 12:46PM To manufacture first indigenously developed IgG antibody detection test kit for Covid-19. The kit is developed by ICMR –NIV. After development the technology for the kits has been transferred to Cadila for mass scale production. This is positive as it could boost the India business topline.
  • Zydus Cadila launches Enzalutamide, making Prostate Cancer therapy highly affordable

    8 May 2020 , 12:06PM Launching of Enzalutamide, a highly effective drug for the treatment of Prostate Cancer
  • Cadila Healthcare

    8 May 2020 , 10:32AM Gets final approval from the U.S. FDA for Deferasirox Tablets for oral suspension. It is used to treat iron overload caused by blood transfusions. It is also used to treat chronic iron overload syndrome caused by a genetic blood disorder; Positive as it would lead to improvement in the US business
  • Cadila Healthcare

    4 May 2020 , 9:50AM Gets USFDA tentative approval for Empagliflozin and Metformin Hydrochloride Tablets Strengths - 5 mg/500 mg, 5 mg/1000 mg, 12.5 mg/500 mg, and 12.5 mg/1000 mg. This medicine is used to control high blood sugar in people with type 2 diabetes. It will be manufactured at the group’s formulations manufacturing facility at SEZ in Ahmedabad. Positive as this would widen the products in the US markets
  • Cadila Health signs agreement to divest stake

    30 Apr 2020 , 3:30PM Divestment of 49% shares of Windlas Healthcare Private Limited
  • Cipla, Cadila, Dr Reddy, Sun Pharma

    30 Apr 2020 , 10:04AM Gilead Sciences has released the results of a Phase III trials of Remdesivir. The results though showed improvement, but the mortality rate in Covid-19 patients was at 7%, which is higher than the mortality rate reported by the US, Germany and India. The Phase 2 trials are underway in the US and the outcome of the same would be a key monitorable. If in case Gilead clears the trials and USFDA approves the drug, the following companies could potentially benefit due to in licensing opportunity - Cadila, CIpla, Sun Pharma (due to Ranbaxy acquisition), Dr Reddy’s amongst others. Reports suggests that Gilead had entered in to a licensing arrangement with some of these companies during the Hepatitis C outbreak to procure medicines and so these have potential in the ongoing Covid-19 pandemic as well.
  • Cipla, Cadila

    23 Apr 2020 , 9:50AM As per media news, get REMS nod from the USFDA for hypertension drug - Ambrisentan tablets with strength of 5-10 mg. Positive
  • Cadila Healthcare

    20 Apr 2020 , 10:38AM Gets a final approval from the USFDA for Baclofen tablets – 5 mg. The medicine is indicated to treat muscle spasms caused by certain conditions such as multiple sclerosis, spinal cord injury/disease. The medicine will be manufactured at the company’s Baddi plant. Positive as it would widen the US product kitty.
  • Cadila Healthcare

    17 Apr 2020 , 11:51AM Has received a final approval from the USFDA for Erlotinib Tablets with strength – 25mg, 100mg, 150 mg. The medicine is used to treat cancer patients and is usually given after other cancer medicines have been tried without success. Medicine would be manufactured at the company’s formulations plant at SEZ at Ahmedabad. The approval would strengthen the company’s US business.
  • Zydus receives final approval from the USFDA for Erlotinib Tablets

    17 Apr 2020 , 11:46AM Erlotinib is a cancer medicine that interferes with the growth of cancer cells and slows their spread in the body
  • Cadila Healthcare

    17 Apr 2020 , 10:51AM Sells 2% stake in subsidiary – Windlas Healthcare; post the deal Windlas would cease to be a subsidiary; the event unlikely to have material impact on cadila performance given the small size of revenues of Windlas.
  • Zydus receives tentative approval from the USFDA for Empagliflozin Tablets

    13 Apr 2020 , 12:36PM Zydus Cadila gets tentative nod from the USFDA to market Empagliflozin Tablets
  • Cadila Healthcare

    13 Apr 2020 , 9:54AM Scales up production for HCQS; Gets USFDA approval for Empagliflozin and Imatinib Mesylate tablets – Positive as these would aid topline growth
  • Zydus receives USFDA nod for Imatinib Mesylate Tablets

    9 Apr 2020 , 11:30AM Zydus gets USFDA nod for Imatinib Mesylate tablets which are used to treat blood & skin cancer
  • Cadila Healthcare

    7 Apr 2020 , 1:05PM Received final approval from the USFDA to market Perphenazine Tablets USP, 2 mg, 4 mg, 8 mg and 16 mg. (US RLD: Trilafon Tablets). The medicine is indicated for the treatment of schizophrenia and for the control of severe nausea and vomiting in adults. The drug will be manufactured at the Baddi facility. Positive as this would further widen the US product portfolio.
  • Zydus receives final approval from USFDA for Perphenazine Tablets USP

    7 Apr 2020 , 12:11PM Zydus gets final nod from the USFDA to market Perphenazine Tablets
  • Cadila Healthcare

    3 Apr 2020 , 10:37AM Zydus Cadila has received final approval from the USFDA to market Lamotrigine Extended-Release Tablets USP in the strengths of 25 mg, 50 mg, 100 mg, 200 mg, 250 mg, and 300 mg. This medication is indicated for the treatment of certain types of seizures and will be manufactured at the group’s manufacturing facility at SEZ, Ahmedabad. This would widen the US product basket , thus adding the topline and hence is positive
  • IPCA, Cadila

    31 Mar 2020 , 9:51AM As per media news, the USFDA has approved the use of HCQS (HydroxyChloroquine) and Chloroquine for the treatment of Covid-19. This is likely to benefit IPCA and Cadila as they are the amongst the largest manufacturers of these drugs
  • Cadila Healthcare gets tentative nod for Carbidopa and Levodopa Capsules

    30 Mar 2020 , 9:50AM Zydus receives tentative approval from the USFDA for Carbidopa and Levodopa Extended-Release Capsules
  • Cadila Healthcare declares dividend

    16 Mar 2020 , 12:52PM Interim Dividend for the financial year 2019-2020
  • Cadila Health approves transfer Animal Health biz to arm

    11 Mar 2020 , 3:14PM Cadila Healthcare approves transfer of Co's Animal Healthcare Business on going concern basis
  • Cadila Healthcare

    6 Mar 2020 , 11:18AM Zydus Cadila has received approval from the Drug Controller General of India (DCGI) for its new drug application for Saroglitazar to treat a particular condition of liver, commonly known as NASH in India – Positive read through for the stock
  • Cadila Healthcare receives DCGI nod for Saroglitazar

    5 Mar 2020 , 3:06PM Cadila Healthcare gets DCGI nod for its New Drug Application
  • Zydus receives Phase I clinical trial permission for ZYBK2 from DCGI

    3 Mar 2020 , 12:27PM Zydus Cadila gets an approval from the Drug Controller General of India (DCGI) to initiate Phase 1
  • Cadila Healthcare

    17 Feb 2020 , 10:34AM Zydus cadila announced that it has initiated an accelerated research programme with multiple teams in India and Europe to develop a vaccine for the novel coronavirus, 2019-nCoV (COVID-19). The development is based in two approaches – one deals with development of a DNA vaccine while the second deals with deals with development of a live attenuated recombinant measles virus vectored vaccine against COVID-19. Positive, if the drug / vaccine is successfully developed and commercialized.
  • Zydus gets nod from USFDA for Mesalamine Suppositories for rectal use

    13 Feb 2020 , 12:44PM The drug is used to treat ulcerative proctitis, a type of bowel disease
  • Cadila Healthcare

    12 Feb 2020 , 10:35AM Zydus Cadila has received the final approval from the USFDA to market Fluocinonide Cream USP, (US - RLD - Vanos Cream) 0.1 %. The drug is used to treat a variety of skin conditions (e.g., psoriasis, eczema, dermatitis, allergies, rash) and will be manufactured at the group's Topical manufacturing facility at Ahmedabad. Positive
  • Cadila Healthcare

    11 Feb 2020 , 10:55AM Company’s topical manufacturing facility located at Ahmedabad has received an Establishment Inspection Report (EIR) from the USFDA pointing towards a successful closure of the audit. The topical manufacturing facility was inspected by the USFDA from 16th to 20th December 2019 and ended with zero 483 observations. This is Positive as the company can commence commercial production from the new plant.
  • Cadila Healthcare

    6 Feb 2020 , 12:44PM Cadila Healthcare: Q3FY2020 Result Update - Not yet out of woods
  • Cadila

    5 Feb 2020 , 1:31PM Alidac Pharmaceuticals a wholly-owned subsidiary’s plant at SEZ, Ahmedabad was inspected by US FDA in between 27th Jan 2020 to 4th Feb 2020. The inspection ended with no observations. The facility manufactures oncology injectables for the regulated markets. No observations received in the inspection is positive.
  • Zydus gets nod from DCGI for treatment of Type II Diabetes

    3 Feb 2020 , 10:48AM Zydus’ Saroglitazar Magnesium has been approvedfor the treatment of diabetes mellitus type 2
  • Cadila Healthcare

    21 Jan 2020 , 10:53AM Cadila: Enters in to a licensing agreement with China Medical System Holdings Limited (CMS) for the development and commercialization of Desidustat – Positive
  • Cadila Healthcare

    27 Dec 2019 , 10:23AM As per media news Zydus Cadila, a group company of Cadila Healthcare is in preliminary talks with several strategic and private equity investors for the sale of its two divisions - anti-infectives (~5% of FY19 revenues) and gynaecology (~2% of FY19 revenues) for a consideration of about Rs 1000 to Rs 1200 crore. The move is a part of the broader strategy to reduce debt after the company had borrowed to finance the Rs 4,600-crore acquisition earlier this year of Heinz India’s consumer wellness business. Positive read thru if the deal goes thru
  • Cadila Healthcare

    23 Dec 2019 , 12:49PM The USFDA inspected the company’s facility at Ahmedabad from 16-20 December 2019. The inspection ended with no observations / no form 483 issued. Ahmedabad plant is a derma facility. Positive read thru
  • Zydus launches affordable oral anti-diabetic tablet Vinglyn

    12 Dec 2019 , 11:53AM Vinglyn and Vinglyn M will be marketed by Zydus Healthcare
  • Cadila Healthcare

    12 Dec 2019 , 11:35AM Zydus Cadila has launched its affordable oral anti-diabetic Vinglyn brand in India. aAs per the company, Vinglyn is now one of the most affordable brands of Vildagliptin for diabetic patients in India. Vinglyn and Vinglyn M will be marketed by Zydus Healthcare Ltd. Positive
  • Cadila Healthcare

    6 Dec 2019 , 11:52AM The Company has filed New Drug Application (NDA) with the Drug Controller General of India (DCGI) for Saroglitazar Mg, used in treatment of liver disease. NASH is a progressive disease of the liver and a significant unmet medical need. There are currently no treatments available for the treatment of NASH. Saroglitazar Mg has previously demonstrated improvement in both liver enzymes along with favorable effects on lipid and glycemic indices in patients with nonalcoholic fatty liver disease in Phase II clinical trials – Positive read through for the stock
  • Zydus Cadila files NDA of Saroglitazar Magnesium for treatment of NASH with DCGI

    5 Dec 2019 , 11:06AM Zydus announces regulatory filing of Saroglitazar Magnesium for treatment of NASH with DCGI
  • Zydus receives tentative nod from the USFDA

    3 Dec 2019 , 1:25PM Zydus receives tentative approval from the USFDA for Lorcaserin Hydrochloride Tablets
  • Cadila Health board approves merger of 4 subsidiaries

    2 Dec 2019 , 12:11PM Cadila Healthcare board approves the draft Scheme of Amalgamation
  • Cadila Healthcare

    25 Nov 2019 , 1:17PM As per media news, the company has received USFDA approval for Defasirox drug, which is used to treat Anemia. Positive
  • Zydus gets USFDA nod for Isosorbide Dinitrate tablets & Desonide cream

    21 Nov 2019 , 12:04PM Zydus receives final approvals from the USFDA for Isosorbide Dinitrate Tablets and Desonide Cream
  • Cadila Healthcare

    18 Nov 2019 , 2:26PM Zydus Cadila has received tentative approval from USFDA to market Apremilast Tablets - 10 mg, 20 mg, and 30 mg. The tablet is used to treat a certain type of arthritis and certain type of skin condition. t is also used to treat mouth sores in people who have Behcet‘s disease. It will be manufactured at the group’s manufacturing facility at Ahmedabad. Positive read thru
  • Zydus announces second Phase 3 trial of Desidustat

    18 Nov 2019 , 12:13PM DREAM—D is the second Phase 3 Trial of Desidustat
  • Cadila Healthcare

    15 Nov 2019 , 12:21PM Cadila Healthcare: Q2FY20 result Update – Weak Health
  • Cadila Healthcare

    14 Nov 2019 , 11:16AM Cadila Healthcare: Q2FY20 results weak operationally; lower tax leads to PAT coming in line with estimates
  • Cadila Healthcare gets nod for Cisatracurium Besylate Injection

    5 Nov 2019 , 12:09PM Zydus receives final approval from the USFDA for Cisatracurium Besylate Injection USP
  • Cadila Healthcare

    4 Nov 2019 , 3:01PM The company has received a warnings letter from the US-FDA relating to its Moraiya formulation facility. The company is confident of responding to US FDA to address the observations within the statutory time permitted in the letter. Negative. The stock is down 4% in trade
  • Cadila Healthcare

    1 Nov 2019 , 11:26AM The company’s manufacturing facility at Baddi has received an Establishment Inspection Report (EIR) from the US –FDA (plant inspected between 15 July 2019 to 19 July 2019). The EIR states that the classification of the facility is No Action Indicated (NAI). This is positive
  • Cadila Healthcare

    14 Oct 2019 , 10:37AM Company’s API manufacturing facility at Dabhasa (largest API facility) successfully completes USFDA inspection (inspected between Oct 7-11, 2019, without any observations) – Positive; This was a CGMP audit and a pre—approval inspection (PAI).
  • Cadila Health's Zydus gets USFDA nod for cholesterol drug

    9 Oct 2019 , 2:36PM Zydus receives final approval from the USFDA for Colesevelam Hydrochloride Tablets
  • Cadila Healthcare to sell rights of Zypitamag drug to Medicure Inc.

    1 Oct 2019 , 10:49AM Cadila: Company to sell its right, title & interest in Zypitamag, along with applicable registrations and intangible assets relating to Zypitamag for US and Canada markets to Medicure – Positive; Cadila will receive upfront payment of $5 million and deferred payment of $2 million to be made over the next four years. Medicure had previously acquired US marketing rights with a profit-sharing arrangement with Cadila. With this acquisition, Medicure retains all profits, with full control of marketing and pricing negotiation for US and Canada markets.
  • Zydus get final nod from USFDA for Clobetasol Propionate Lotion

    26 Sep 2019 , 12:05PM Zydus receives final approval from the USFDA for Clobetasol Propionate Lotion
  • Cadila Healthcare gets EIR for Ankleshwar API unit

    23 Sep 2019 , 12:27PM Cadila Healthcare API manufacturing facility located at Ankleshwar gets an Establishment Inspection Report (EIR)
  • Zydus gets final nod from USFDA for Ranolazine ER Tablets

    21 Aug 2019 , 2:21PM The drug is used to treat chronic angina and may be used with other medicines that are used for heart problems and blood pressure control
  • Zydus gets final nod from USFDA for Ranolazine ER Tablets

    21 Aug 2019 , 2:20PM The drug is used to treat chronic angina and may be used with other medicines that are used for heart problems and blood pressure control
  • Zydus Cadila completes Phase III trials of Saroglitazar Magnesium

    2 Aug 2019 , 11:49AM Zydus announces completion of Phase III trials of Saroglitazar Magnesium in Type 2 Diabetes Mellitus
  • Zydus Cadila completes enrollment in three Phase-III trials of Saroglitazar Magnesium

    18 Jul 2019 , 12:09PM Zydus announces completion of enrollment in three Phase III trials of Saroglitazar Magnesium in NASH
  • Cadila Q4FY2019 : Sales above estimate but profit below estimate

    29 May 2019 , 4:40PM Sales for the quarter reported 14.9% growth to Rs 3733 crore (above estimate). Operating profit declined by 8% to Rs 800 crore (below estimate). Adj. PAT declined by 24.5% to Rs 458 crore (below estimate). Post management call (on 29 May 2019 at 4.30 pm) we shall review our estimates and come out with detailed note. We currently have hold rating on the stock.
  • Zydus Cadila gets USFDA nod to market Esomeprazole Magnesium Delayed-Release Capsules

    23 May 2019 , 11:26AM Cadila's Zydus receives final approval from the USFDA for Esomeprazole Magnesium Delayed-Release Capsules USP
  • Zydus receives final nod from USFDA for Chlorthalidone Tablets USP

    13 May 2019 , 11:27AM Cadila's Zydus receives final approval from the USFDA for Chlorthalidone Tablets USP
  • Moraiya facility receives Form 483 with 14 observation from USFDA

    6 May 2019 , 10:51AM Cadila – Co’s Moraiya facility receives Form 483 with 14 obs from the USFDA - Negative; Company currently has ~33-35 ANDAs pending approval from this site; Moraiya facility contributes ~40-45% to US business; Stock to remain under pressure till clarity emerges
  • Cadila Healthcare gets 14 observations from USFDA

    6 May 2019 , 10:36AM USFDA issues 14 observations for Cadila Healthcare's Moraiya facility
  • Zydus Cadila gets final nod from USFDA to market tablets

    30 Apr 2019 , 12:38PM Cadila's Zydus receives final approval from USFDA for Bosentan Tablets and Trientine Hydrochloride Capsules
  • Zydus gets tentative nod from USFDA for Lacosamide Tablets

    8 Apr 2019 , 12:39PM Zydus Cadila receives tentative approval from the US health regulator to market Lacosamide Tablets
  • Cadila gets tentative nod from USFDA

    8 Apr 2019 , 10:45AM Cadila: Company received tentative approval from USFDA to market Tofacitinib tablets, used to treat moderate to severe forms of rheumatoid arthritis – Positive read thru.
  • Zydus receives tentative approval from USFDA for Tofacitinib Tablets

    8 Apr 2019 , 10:24AM Zydus Cadila get nod to market Tofacitinib tablets to treat moderate to severe forms of rheumatoid arthritis
  • Cadila Health gets 1 observation from USFDA

    3 Apr 2019 , 2:26PM Cadila Healthcare is confident of addressing the observation at the earliest
  • Zydus receives tentative nod from USFDA for Mirabegron tablets

    2 Apr 2019 , 1:01PM Zydus receives tentative approval from the USFDA for Mirabegron Extended-Release Tablets
  • Zydus receives final approval from the USFDA for Ambrisentan Tablets

    29 Mar 2019 , 11:21AM Zydus Cadila gets final USFDA nod to market Ambrisentan Tablets USP, to treat high blood pressure in the lungs
  • Zydus gets USFDA nod for Lurasidone Hydrochloride tablets

    22 Mar 2019 , 2:43PM Zydus receives final approval from the USFDA for Lurasidone Hydrochloride Tables
  • Zydus receives final approval from USFDA

    19 Mar 2019 , 2:41PM Zydus receives final approval from the USFDA for Acyclovir Ointment
  • Zydus receives final nod from the USFDA

    13 Mar 2019 , 12:02PM Zydus receives final approval from the USFDA for Potassium Chloride Extended-Release Capsules USP
  • Zydus receives final approval from USFDA for Atenolol and Chlorthalidone tablet

    12 Mar 2019 , 12:23PM Zydus Cadila gets USFDA nod to market Atenolol and Chlorthalidone Tablets USP
  • Zydus receives USFDA nod for Rivastigmine tablets

    5 Mar 2019 , 12:59PM Zydus receives USFDA approval for its first transdermal product, Rivastigmine Transdermal System
  • Zydus gets USFDA nod for seizure drug Carbamazepine

    8 Feb 2019 , 12:01PM Zydus receives final approval from USFDA for Carbamazepine Extended-Release tablets
  • Cadila gets final nod from USFDA for antipsychotic drug

    8 Jan 2019 , 12:31PM Global pharmaceutical company receives final approval from the USFDA to market Aripiprazole Tablets
  • Cadila Healthcare gets USFDA nod to market acne drug

    31 Dec 2018 , 10:12AM Zydus receives final approval from the USFDA for Clindamycin Phosphate and Benzoyl Peroxide Gel
  • Zydus Cadila gets USFDA nod for two drugs

    24 Dec 2018 , 12:41PM Zydus receives approvals from the USFDA for Doxycycline Hyclate Delayed-Release Tablets and Febuxostat Tablets
  • Cadila gets USFDA nod to market Albendazole tablets

    17 Dec 2018 , 10:28AM Zydus receives approvals from the USFDA for Albendazole Tablets and Pregabalin Capsules
  • Cadila Healthcare arm gets USFDA nod for ulcer treatment

    11 Dec 2018 , 1:09PM Liva Pharmaceuticals subsidiary of Cadila Healthcare receives USFDA approval for Ranitidine Injection
  • Cadila Healthcare gets USFDA nod for Linagliptin, Lansoprazole tablet

    29 Nov 2018 , 12:36PM Zydus receives approvals from the USFDA for Lansoprazole Tablets and Linagliptin tablets
  • Zydus Cadila gets USFDA nod for two drugs

    22 Nov 2018 , 2:38PM Zydus receives approvals from the USFDA for Atorvastatin Calcium Tablets and Dimethyl Fumarate Delayed-Release Capsules
  • Zydus gets tentative nod from USFDA for Deferasirox Tablets

    20 Nov 2018 , 12:25PM Zydus Cadila has receives the tentative approval from the USFDA to market Deferasirox Tablets
  • Zydus gets final USFDA nod for HIV drug

    16 Nov 2018 , 1:04PM Zydus receives final USFDA nod for Abacavir & Lamivudine tablets, Fondaparinux Sodium injection
  • Cadila Q2FY2019 profit better than expectation

    5 Nov 2018 , 10:57AM Sales for the quarter declined by 8.4% to Rs. 2961 crore, mainly on account of sharp decline in US business (on account of high base of gLialda in Q2FY2018) Operating profit declined by 19.7% to Rs. 19.7% to Rs. 688 crore; OPM declined by 327 bps to 23.2% Adj. PAT declined by 16.9% to Rs. 418 crore.
  • Cadila gets EIR from USFDA

    5 Oct 2018 , 11:32AM Cadila biologics manufacturing facility at Ahmedabad receives an establishment inspection report from the USFDA; audit was completed with zero form 483 observations – Positive for Cadila; We have a buy recommendation on the stock with PT of Rs 450.
  • Cadila gets nod for Risedronate Sodium Tablets

    14 Sep 2018 , 11:15AM Zydus receives final approval from the USFDA for Risedronate Sodium Delayed-Release Tablets
  • Cadila receives nod from USFDA

    14 Sep 2018 , 10:14AM Cadila Healthcare: Received approval from USFDA for Risedronate Sodium Delayed-Release Tablets 35 mg. It will be manufactured at the group’s formulations manufacturing facility at Moraiya, Ahmedabad. This medicine is used to treat osteoporosis in women. Positive for Stock
  • Cadila gets USFDA tentative nod for Sitagliptin Tablets

    11 Sep 2018 , 2:09PM Cadila gets USFDA tentative approval for Sitagliptin Tablets (gJanuvia – used to treat diabetes); it will be manufactured at formulations manufacturing facility at SEZ, Ahmedabad – Positive for Cadila.
  • USFDA grants Zydus tentative nod for diabetes pill

    11 Sep 2018 , 11:42AM Zydus receives tentative approval from the USFDA for Sitagliptin Tablets
  • SFDA grants Zydus tentative nod for diabetes pill

    11 Sep 2018 , 11:40AM Zydus receives tentative approval from the USFDA for Sitagliptin Tablets
  • USFDA issues Form 483 with five observations

    7 Sep 2018 , 11:05AM USFDA issues Form 483 with five observations to Cadila healthcare’s subsidiary Liva Pharmaceuticals' injectables manufacturing facility – Sentimentally negative.
  • Zydus gets USFDA nod for antiviral drug

    5 Sep 2018 , 12:13PM Zydus receives final approval from the USFDA for Acyclovir Sodium Injection
  • Cadila gets 5 observations from USFDA

    29 Aug 2018 , 2:20PM USFDA conducted the inspection from August 20-28. Liva is a 100% subsidiary of Cadila Healthcare
  • USFDA inspect injectables facility of Liva Pharma

    29 Aug 2018 , 1:58PM Cadila: USFDA inspected (from 20th August 2018 to 28th August 2018) the injectables manufacturing facility of Liva Pharmaceuticals Ltd, located at Vadodara; Liva is a 100% subsidiary of Cadila; This inspection was a product specific Pre Approval Inspection, which concluded with 5 observations; At present Liva does not export any products to the US market – Neutral read thru
  • Cadila successfully completes USFDA inspection

    24 Aug 2018 , 3:23PM Cadila Healthcare's Biologics manufacturing facility successfully completes USFDA inspection
  • Cadila net profit at Rs467 cr

    13 Aug 2018 , 3:34PM Cadila Q1FY2019: High other income, forex gain and low tax boost profit; numbers below expectatio
  • Cadila gets USFDA nod for tablets

    30 Jul 2018 , 11:53AM Cadila Healthcare gets USFDA tentative approval for Vardenafil Hydrochloride Tablets
  • Zydus Cadila bags 4 approvals from USFDA

    18 Jul 2018 , 11:50AM Zydus Cadila receives four consecutive final approvals from the USFDA to market Olanzapine Tablets USP, Glipizide Extended-Release Tablets, Voriconazole for Injection and Fluocinonide Topical Solution USP
  • Zydus gets USFDA nod for anti-bacterial drug

    17 Jul 2018 , 12:22PM Zydus receives final approval from the USFDA for Clindamycin Phosphate Topical Solution USP
  • Cadila gets USFDA approval for Triamterene & Hydrochlorothiazide Tablets

    2 Jul 2018 , 11:47AM We have a buy rating on the stock with PT of Rs 450.
  • Cadila gets USFDA approval for Triamterene & Hydrochlorothiazide Tablets

    2 Jul 2018 , 11:42AM We have a buy rating on the stock with PT of Rs 450.
  • Cadila up on USFDA inspection

    6 Jun 2018 , 12:11PM Cadila Healthcare rises over 3% at Rs359.85, after USFDA completes inspection of company's wholly-owned subsidiary with no observation
  • Zydus gets final nod from USFDA for anti-bacterial drug

    4 Jun 2018 , 10:53AM Zydus Cadila receives the final approval from the USFDA to market Doxycycline Hyclate Capsules USP, 50 mg and 100 mg
  • Cadila receives final approval from USFDA

    4 Jun 2018 , 9:57AM Positive read through for Zydus Cadila.
  • Cadila gets USFDA nod for Carbidopa tablets

    10 May 2018 , 12:23PM Cadila Healthcare receives final approval from the USFDA to market Carbidopa tablets
  • Cadila gets USFDA final approval

    7 May 2018 , 11:03AM Positive for Cadila as it gets USFDA final approval from for Succinylcholine Chloride injection and tentative approval for Plerixafor Injection.
  • Weak performance to continue for Pharma

    9 Apr 2018 , 10:36AM Weak performance to continue, maintain cautious stance for Pharma
  • Cadila Healthcare clears USFDA inspection

    2 Apr 2018 , 10:46AM Positive for Cadila
  • Cadila gets USFDA approval for gToprol XL

    26 Mar 2018 , 11:51AM Negative for Dr Reddy as Cadila gets USFDA approval for gToprol XL (Metoprolol Succinate Extended Release) tablets but positive for Cadila.
  • Cadila jumps 5% after USFDA drug nod

    26 Mar 2018 , 11:34AM Cadila Healthcare rises by 5% at Rs389.50, after receiving final approval from the US drug regulator for Metoprolol Succinate extended-release tablets
  • Cadila gets USFDA approval for drug

    13 Mar 2018 , 1:19PM Cadila Healthcare receives final approval from the US drug regulator for its Tizanidine tablets
  • Cadila partners with Medicure

    8 Mar 2018 , 12:28PM Positive read through for Cadila as it partners with Medicure to launch its New Drug application (NDA) product Zypitamag (pitavastatin) on the US.
  • Cadila gets USFDA approval for Dexmedetomidine Hydrochloride injection

    1 Mar 2018 , 9:22AM Positive read through for Cadila as Cadila gets USFDA approval for Dexmedetomidine Hydrochloride injection used to sedate without risk of respiratory depression.
  • Cadila sucessfully completes USFDA inspection

    12 Feb 2018 , 12:05PM Cadila Healthcare its Moraiya facility successfully completed US drug regulator's inspection
  • Cadila completes USFDA audit

    12 Feb 2018 , 10:27AM Huge positive read through for Cadila as it successfully completes USFDA audit with zero observation.
  • Cadila gets USFDA nod for Valacyclovir Tablets

    1 Jan 2018 , 2:35PM Cadila Healthcare receives final approval from the US drug regulator for Valacyclovir Tablets USP
  • Cadila gets USFDA approval for Valacyclovir tablets

    1 Jan 2018 , 9:36AM Cadila gets USFDA approval for Valacyclovir tablets, used to treat cold sores (herpes) and shingles
  • Cadila gets final nod from US drug regulator

    21 Dec 2017 , 12:26PM Cadila surges over 3% to Rs434.3, after receiving final approval from the US drug regulator for Nifedipine extended-release tablets
  • Cadila gets USFDA nod to market drug for high blood pressure

    29 Nov 2017 , 12:20PM Cadila Healthcare receives final approval from the USFDA for Candesartan Cilexetil and Hydrochlorothiazide Tablets
  • Cadila gets USFDA nod for tablets to treat high blood pressure

    29 Nov 2017 , 11:03AM Positive for Cadila as it receives final approval from the USFDA for Candesartan Cilexetil and Hydrochlorothiazide Tablets, used to treat high blood pressure and shall be manufactured at Moraiya facility.
  • Cadila gets USFDA nod for Topiramate Extended-Release Capsules

    27 Nov 2017 , 11:41AM Positive for Cadila.
  • Cadila gets USFDA nod for acne drug

    24 Nov 2017 , 2:33PM Cadila Healthcare receives approval from USFDA for Minocycline Hydrochloride Extended - Release tablets
  • Cadila receives USFDA approval for Minocycline Hydrochloride

    24 Nov 2017 , 10:24AM Positive news for Cadila as it receives approval from the USFDA for Minocycline Hydrochloride Extended - Release Tablets and shall be manufactured at formulation facility in Moraiya
  • Cadila gets USFDA nod to market Ethacrynate sodium

    21 Nov 2017 , 8:53AM Positive news for Cadila as it gets USFDA approval to market Ethacrynate sodium for injection.
  • Cadila Healthcare gets USFDA final approval for drug

    20 Nov 2017 , 12:02PM Zydus Cadila receives final approval from the US Food & Drug Administration (USFDA) to market Ethacrynate Sodium for Injection USP, 50 mg/vial
  • Cadila Healthcare reports strong Q2 growth

    15 Nov 2017 , 12:24PM Cadila: High tax rate guidance to affect profitability
  • Cadila reports strong Q2 operational performance

    14 Nov 2017 , 12:33PM Cadila reports strong operational performance driven by strong growth across geographies; gLialda 180day exclusivity was one of the key growth driver.
  • Cadila’s subsidiary Nesher pharma, gets USFDA nod for tablets to treat ADHD

    2 Nov 2017 , 3:01PM Positive news for Cadila as subsidiary Nesher pharma, gets USFDA approval for Dextroamphetamine sulfate and Amphetamine sulfate tablets to treat ADHD (Attention Deficit Hyperactivity Disorder) and Narcolepsy and shall be manufactured at St Louis US facility.
  • Cadila gets USFDA approval for drug to treat infectious disorders

    31 Oct 2017 , 3:19PM Positive news for Cadila as it gets USFDA approval for Doxycycline Hyclate Tablets USP.
  • Cadila gets USFDA nod for skin ointment

    30 Oct 2017 , 12:48PM Cadila Healthcare gets final approval from the U.S. drug regulator to market Clobetasol Propionate ointment
  • Cadila gets USFDA nod for Tamoxifen Citrate tablets

    30 Oct 2017 , 8:41AM Positive news for Cadila Healthcare. The Tamoxifen Citrate tablets will be used in treatment of breast cancer in women and men
  • Cadila gets USFDA nod for Desvenlafaxine extended-release tablets

    12 Oct 2017 , 1:42PM Cadila Healthcare rises over 2% to Rs503, after US drug regulator gave its final approval to market Desvenlafaxine extended-release tablets
  • Cadila gets USFDA nod for drugs

    9 Oct 2017 , 12:14PM Cadila receives the final approval from USFDA to market Amitriptyline Hydrochloride Tablets
  • Cadila gets USFDA for tablets used to treat depression

    9 Oct 2017 , 8:42AM Cadila gets USFDA approval for Amitriptyline Hydrochloride Tablets USP, used to treat depression. The drug shall be manufactured at Ahmedabad SEZ formulation facility – Positive for Cadila.
  • Zydus Cadila gets final nod for doxycycline tablets

    29 Sep 2017 , 3:10PM Zydus Cadila receives final approval from the US health regulator to market doxycycline tablets
  • Zydus bags approval for Indomethacin capsules

    27 Sep 2017 , 3:00PM Zydus Cadila receives final approval from USFDA to market Indomethacin Extended-Release Capsules USP, 75 mg
  • Cadila gets USFDA nod to treat high blood pressure

    25 Sep 2017 , 12:26PM Cadila: Gets USFDA approval for Amlodipine and olmesartan medoxomil tablets, used to treat used to treat high blood pressure (hypertension) – Positive for Cadila.
  • Cadila gets USFDA approval for Itraconazole capsules

    22 Sep 2017 , 8:56AM Cadila gets USFDA approval for Itraconazole capsules (used to treat fungal infections) which shall be manufactured at formulation facility at Moraiya – Positive for Cadila.
  • Cadila gets USFDA approval for Modafinil

    18 Sep 2017 , 9:36AM Cadila received USFDA approval for Modafinil tablets (used to improve wakefulness) & Solifenacin Succinate tablets (used to treat overactive bladder)– Positive read-thru
  • Cadila up after inspection of Moraiya facility

    7 Sep 2017 , 3:14PM Cadila rises by 5% to Rs519.9, after its Moraiya facility successfully completed US drug regulator's inspection
  • Cadila Healthcare receives USFDA approval

    4 Sep 2017 , 11:31AM Cadila Healthcare receives final approval from the US drug regulator to market a drug
  • Cadila Healthcare Ltd. received EIR from USFDA

    29 Aug 2017 , 11:42AM Cadila Healthcare Ltd. received EIR: Positive for stock
  • Cadila's receives USFDA for Candesartan Cilexetil tablets

    24 Aug 2017 , 12:20PM Cadila's receives USFDA final approval for hypertension drug Candesartan Cilexetil tablets from Moraiya unit – Positive for Cadila
  • Cadila gets USFDA nod for Pindolol tablets

    22 Aug 2017 , 2:58PM USFDA approves manufacturing of Pindolol tablets (used to treat hypertension) by Cadila – Positive for Cadila.
  • Cadila & Torrent Pharma potential merger foreseen

    22 Aug 2017 , 9:34AM As per media reports, Cadila and Torrent pharma are evaluating potential merger between the companies. However, both the companies have strongly denied it.
  • USFDA approval: Positive for Cadila

    17 Aug 2017 , 11:37AM Cadila gets USFDA approval for Telmisartan and Hydrochlorothiazide tablets
  • Cadila: Weak operating performance in Q1FY18

    14 Aug 2017 , 2:34PM Maintain Hold with unchanged TP of Rs 485.
  • Cadila gets USFDA’s nod to market Diltiazem Hydrochloride capsules

    9 Aug 2017 , 2:10PM USFDA approves Cadila to market Diltiazem Hydrochloride capsules, used to treat high blood pressure, angina (chest pain) and certain heart rhythm disorders.
  • Cadila gets USFDA nod for Abacavir & Lamivudine

    8 Aug 2017 , 1:53PM Cadila receives tentative approval from USFDA for Abacavir & Lamivudine Tablets - positive read thru.
  • Cadila healthcare gets USFDA approval for gNamenda

    5 Aug 2017 , 2:57PM Cadila healthcare: Gets USFDA approval for gNamenda (Memantine hydrochloride) extended release capsules, used to treat moderate to severe Alzheimer's disease.
  • Cadila gets FDA nod for sclerosis drug; stk up

    17 Jul 2017 , 11:32AM Cadila Healthcare rises by 3% to Rs545.4, after company receives tentative nod from the US drug regulator to market Fingolimod Capsules, 0.5 mg
  • Cadila enters into agreement with Phibro

    6 Jul 2017 , 11:22AM Zydus Cadila enters into a long-term arrangement with Phibro Animal Health Corporation to license Phibro’s
  • Cadila gets USFDA nod for Disintegrating tablets

    30 Jun 2017 , 10:27AM Cadila Healthcare receives final approval from USFDA to market Phentermine Hydrochloride Orally Disintegrating Tablets
  • Zydus Cadila bags approval for Oxybutynin Chloride tablets

    28 Jun 2017 , 12:09PM Zydus Cadila receives the final approval from USFDA to market Oxybutynin Chloride Extended-Release Tablets in the strengths of 5 mg, 10 mg and 15 mg
  • Cadila receives USFDA approval for Acyclovir

    15 Jun 2017 , 12:43PM Cadila Healthcare receives the final approval from USFDA to market Acyclovir for injection USP
  • Cadila hits 52-week high on getting EIR from USFDA

    6 Jun 2017 , 11:08AM Cadila Healthcare rises by 4% to Rs510, after the company said its Baddi facility gets EIR from US drug regulator
  • Cadila gets USFDA nod to market Mirtazapine

    5 Jun 2017 , 1:54PM Zydus Cadila receives US health regulator’s nod to market Mirtazapine, orally disintegrating tablets, an anti-depressant, in the American market
  • Cadila Healthcare hits record high

    2 Jun 2017 , 12:06PM Cadila Healthcare rises over 7% to Rs504.8, after Moraiya plant receives first product approval post successful audit by the US drug regulator.

Key fundamentals

Evaluate the intrinsic value of Zydus Lifesciences Ltd stock 

Name March-24 March-23 March-22 March-21 March-20
Assets 21890 18461.9 15903.1 16660.4 14214.6
Liabilities 21890 18461.9 15903.1 16660.4 14214.6
Equity 100.6 101.2 102.4 102.4 102.4
Gross Profit 4058.7 2454.4 1918.1 2308.7 1423.1
Net Profit 3441.5 1529.2 857.9 1476.2 1412.9
Cash From Operating Activities 1999.1 1078.2 1310.7 2225.3 1180.6
NPM(%) 31.81 17.51 10.74 18.97 22.25
Revenue 10818.7 8731.6 7981.9 7780 6347.4
Expenses 6760 6277.2 6063.8 5471.3 4924.3
ROE(%) 15.76 7 3.93 6.76 6.47

Shareholding Pattern

Corporate Action

XD-Date Dividend-Amount Dividend-% Dividend Yield(%GE) Price on that day
26 Jul 2024 3 300 0.34 1051.4
28 Jul 2023 6 600 0.34 508.05
28 Jul 2022 2.5 250 0.34 356.85
28 Jul 2021 3.5 350 0.34 626.85
23 Mar 2020 3.5 350 0.34 258.1
25 Jul 2019 3.5 350 0.34 263.75
31 Jul 2018 3.5 350 0.34 382.2
16 Mar 2017 3.2 320 0.34 443.65
17 Mar 2016 3.2 320 0.34 335.7
30 Jul 2015 12 240 0.34 1689.15
17 Jul 2014 9 180 0.34 911.15
11 Jun 2013 7.5 150 0.34 775.15
26 Jul 2012 7.5 150 0.34 758.85
07 Jul 2011 6.25 125 0.34 871.6
15 Jul 2010 5 100 0.34 561
16 Jul 2009 4.5 90 0.34 308.2
10 Jul 2008 4.5 90 0.34 272.05
12 Jul 2007 4 80 0.34 322.2
13 Jul 2006 6 120 0.34 702.35
14 Jul 2005 6 120 0.34 434.45
14 Jul 2004 6 120 0.34 520.75
24 Sep 2003 3.5 70 0.34 248.35
11 Sep 2002 0 70 0.34 137.65
0 0 0.34 125.6
18 Jun 2001 0 60 0.34 101.7
0 60 0.34 130.15

Peers

Other companies within the same industry or sector that are comparable to Zydus Lifesciences Ltd

Company Price Price (% change) pe(x) EV/EBITDA(x) ROE(%) ROCE(%)
Albert David Ltd 840.85 0.23 11.87 505.57 1321.50 1.37
Lotus Eye Hospital and Institute Ltd 81.36 2.94 339.00 1842.24 14.01 0.61
Vaishali Pharma Ltd 13.72 -0.15 457.33 949.56 2.76 0.00
Astec Lifesciences Ltd 693.05 -1.61 0.00 1737.07 -687.11 0.00

Company Info

1995 - The Company was incorporated as Cadila Healthcare Private Ltd. on May 15, under the company act, 1956 and subsequently the Company was converted into a public company and then renamed as Cadila Healthcare Ltd. effective from Juy 17, 1996. - The name "Cadila" shall be used only for "Cadila Healthcare Limited" (Zydus Cadila), "Cadila Pharmaceuticals Limited" (CPL) and "Cadila Laboratories Limited" (CLL). - The Company is flagship company of Zydus Cadila Group. - The Company's operations include pharmaceuticals (human formulations, veterinary formulations and bulk drugs); diagnostics, herbal products, skin care products and other OTC products. - The Company has 6 subsidiaries Indon Healthcare Ltd., Zydus Pharmaceuticals Ltd., Zudus Aqrovet Ltd., Zoom Properties Pvt. Ltd., Zydus International Pvt. Ltd., Ireland and Zydus Healthcare S.A. (Pvt) Ltd., South Africa. - Zydus Cadila signed an agreement with Anda Biologicals, France, for Marketing and distribution of diagnostic kits. Anda to appoint a max. of two distributors in India. 1996 - Zydus Cadila signed an agreement with Centeon L.L.C., USA and Centeon Pharama GMBH, Germany for Exclusive rights to sell and distribute plasma products in India and Nepal. - In May, Zydus Cadila signed an agreement with Acta Services Srl., Rome for distribution of Diagnostic instrument Acto 1 Analyser manu. By Acta. - In June, Zydus Cadila signed an agreement with China Resources Gulin Pharma, Works, China, for exclusive supply of Artesunate Granules to Zydus Cadila. - In July, Zydus Cadila signed an agreement with Shimizu Chemical Corporation, Japan, for Marketing of specified products by Zydus Cadila in India. 1997 - A Scheme of Arrangement and Amalgamation was sanctioned by honorable High Court of Gujarat by order passed on May 2 issued on August 16th. - Zydus Cadila would issued 1,48,423 fully paid-up equity shares of Rs 10/- each to the shareholders of Patel Group in exchange for the assets transferred to them of Transferor companies. - Zydus Cadila has also tied-up with Regional Research Laboratory Jammu, to develop Enzymatic Resolution for Paroxetine HCL and some other Enzymatic products. 1998 - In February, Zydus Cadila signed an agreement with Apotex SA Pty. Ltd. for manufacturer of Amoxycillin, Ampicillin, Co - trimoxazole, paracetamol. - Zydus Cadila has also entered into a joint venture with Korea Green Cross Corporation, Korea, to manufacture and market recombinant Hepatitis B vaccine in India. 1999 - In April, Zydus Cadila signed an agreement with Ethical Holdings Plc, Beta Pharma, and Ethical Pharma South America S.A. for Know-how Licence Agreement to manufacture, marketing and sell transdermal pharmaceutical formulations. - In September, Zydus Cadila signed an agreement with Cherry Valley Farms Ltd., UK for supply of vaccine eggs. - Zydus Cadila has entered into a 50:50 joint venture with Byk Gulden of Germany, a renowned, research-oriented Pharma company of Germany and the world-wide patent holder of the novel proton pump inhibitor, "Pantoprazole". - During the year under report, the Company had issued 2,00,000 12% Cumulative Redeemable Preference shares of Rs. 100/- each fully paid to the members of the Company, which are redeemable at par on 1st July, 2001. - During the year under report, Indon Healthcare Limited and Zydus Aqrovet Limited, have become wholly owned subsidiaries of the company. - During the year under report, the Company has undertaken to set up a new project for manufacturing the bulk drug-Losartan at Ankleshwar. - The Company laid the foundation for a new feed supplement plant, at Vatwa. The feed supplement for poultry and cattle has been developed by tie company's R & D bio-tech department. - The Company has set up a joint venture company to manufacture the break-through molecule Pantoprazole. The Company is also undertaking discovery research projects with Byk Gulden as a pan of the Joint Venture. - The Company has entered into a technical-cum-marketing tie-up with the Swiss Serum and Vaccine Institute, Berne, Institute to launch a range of vaccines in India. - The Company has entered into a joint venture with the Haffkine institute to undertake research in the field of human vaccine and equine sera. - A new State-of-Art Research & Development centre being set-up with the capital cost of approximately Rs. 25.00 crores in the Village: Moraiya. Taluka:Sanand, Dist.: Ahmedabad. - During the year under report the Company has launched several new products in the market : Vac Typh, HB Vac, Xylodac, Losartan, Losacar was the first to be launched in India & Matergam P. - The Company has set up manufacturing premises to manufacture the feed supplement - Improval at GIDC Vatwa. - Shir Pranlal Bhogilal was appointed as an additional Director of the Company with effect from 15th December, 1998 pursuant to Section 260 of the Companies Act, 1956. - Shri Mukesh M. Patel Director of the Company retires by rotation and he is eligible for reappointment. - A new welfare policy has been introduced for employees of the Company. 2000 - The Company is setting up wholly owned subsidiaries abroad and plans to acquire overseas companies to market products. - The Company has entered into License Agreement for phased manufacture and technical know-how transfer with Swiss Serum and Vaccine Institute, Switzerland for the manufacture of Purified Cuck Embroy Vaccine. - The Country's fifth largest pharmaceutical company, is considering offering stocks to its employees through an employees' stock option scheme. - The Company has launched two drugs for the treatment of human immunodeficiency virus. - The Bulk Drugs at Ankleshwar in Gujarat has an ISO 9002 certification for the manufacture and supply of a number of molecules. - Public Issue of 1,48,86,000 No. of Equity shares ("Issue") of Rs 5/- each issued for cash at a premium of Rs [] per share aggregating Rs [] million. The Issue includes a Book Built Portion of 1,33,97,400 No. of equity shares and a Fixed price portion of 14,88,600 No. of Equity Shares. - Authorised share capital of the Company is Rs 500 million divided into 9,00,00,000 No. of Equity Shares of Rs 5/- each and 5,00,000 Preference Shares of Rs 100/- each. - During the year under report, the Company has been recognise as a "Prestigious Unit" and granted adhoc eligibility for Sales Tax deferment by the Industries Commissionerate, Gandhinagar, under New Incentive Policy - Capital Investment Incentive to Premier/ Prestigious unit scheme 1995-2000. - During the year under report Zydus Pharmaceuticals Limited and Zoom Properties Limited have become Wholly Owned Subsidiaries of the Company. - The Company has formed a JV Company in the name of Zydus Byk Healthcare Limited with an equal participation in collaboration with Byk Gulden Lomberg Chemische Fabrik GmbH, Germany, for manufacturing of Bulk Drugs, Formulations and R & D. - The Company has also formed a JV Company in the name of Sarabhai Zydus Animal Health Ltd. in collaboration with Ambalal Sarabhai Enterprises Ltd., Baroda, with an equal participation to carry on the business of animal health segments. - The company has also entered into a technical collaboration with Ethical Holdings of U.K. to manufacture and market transdermal patches in India. - The Company launched block-buster molecules Atorvastatin (Atorva), Lamivudine (Lamidac 100) and Celecoxib (Zycel), Meloxicam (Mel-OD) and Carvedilol (Carvil) during the year. - The company was the first to launch the anti-hypertensive drug Losartan in India. - Currently ranked 6th largest pharmaceutical company in India, Cadila Healthcare is one of the fastest growing pharmaceutical companies in the country. - It has also entered into a technical collaboration with Ethical Holdings of the UK to manufacture and market transdermal patches in India. - Zydus Cadilla has also entered into a technical collaboration with Ethical Holdings of the UK to manufacture and market transdermal patches in India. - Cadlia Healthcare (CHL) has signed an MoU with Rs 54 crore Recon Limited, whereby it will acquire all the 8 formulation brands of the Bangalore based comapny, as well as its distribution network. - The new company, `Recon Healthcare Ltd' is now a subsidiary of Zydus Cadila with Zydus holding 90 per cent stake. - Cadila Healthcare Ltd is setting up wholly owned subsidiaries abroad and plans to acquire overseas companies to market products. - Cadila also launched zidovudine, which is imported and marketed under the brand name Zydowin. Zidovudine, commonly called AZT, is an AIDS-retardant drug made by Glaxo Wellcome. - Zydus Alidac, the marketing arm of Cadila Healthcare Ltd., has launched www.penegra.org. -The Ahmedabad-based Cadoila Healthcare has completed the phase-III clinical trials and the bioequivalence study of the wonder drug sildenafil citrate (Viagra). 2001 - Cadila Healthcare has signed a three year collaborative R&D agreement with Danish biotech company Pantheco in the field of anti-bacterials. - The neurosciences division launched by the company has introduced anxiolytic paroxetine for the first time in the country. - Cadila Healthcare Ltd has posted a 14.75 per cent increase in net profit at Rs 21.86 crore for the quarter ended September 30, 2001.YEAR EVENTS 1995 - The Company was incorporated as Cadila Healthcare Private Ltd. on May 15, under the company act, 1956 and subsequently the Company was converted into a public company and then renamed as Cadila Healthcare Ltd. effective from Juy 17, 1996. - The name "Cadila" shall be used only for "Cadila Healthcare Limited" (Zydus Cadila), "Cadila Pharmaceuticals Limited" (CPL) and "Cadila Laboratories Limited" (CLL). - The Company is flagship company of Zydus Cadila Group. - The Company's operations include pharmaceuticals (human formulations, veterinary formulations and bulk drugs); diagnostics, herbal products, skin care products and other OTC products. - The Company has 6 subsidiaries Indon Healthcare Ltd., Zydus Pharmaceuticals Ltd., Zudus Aqrovet Ltd., Zoom Properties Pvt. Ltd., Zydus International Pvt. Ltd., Ireland and Zydus Healthcare S.A. (Pvt) Ltd., South Africa. - Zydus Cadila signed an agreement with Anda Biologicals, France, for Marketing and distribution of diagnostic kits. Anda to appoint a max. of two distributors in India. 1996 - Zydus Cadila signed an agreement with Centeon L.L.C., USA and Centeon Pharama GMBH, Germany for Exclusive rights to sell and distribute plasma products in India and Nepal. - In May, Zydus Cadila signed an agreement with Acta Services Srl., Rome for distribution of Diagnostic instrument Acto 1 Analyser manu. By Acta. - In June, Zydus Cadila signed an agreement with China Resources Gulin Pharma, Works, China, for exclusive supply of Artesunate Granules to Zydus Cadila. - In July, Zydus Cadila signed an agreement with Shimizu Chemical Corporation, Japan, for Marketing of specified products by Zydus Cadila in India. 1997 - A Scheme of Arrangement and Amalgamation was sanctioned by honorable High Court of Gujarat by order passed on May 2 issued on August 16th. - Zydus Cadila would issued 1,48,423 fully paid-up equity shares of Rs 10/- each to the shareholders of Patel Group in exchange for the assets transferred to them of Transferor companies. - Zydus Cadila has also tied-up with Regional Research Laboratory Jammu, to develop Enzymatic Resolution for Paroxetine HCL and some other Enzymatic products. 1998 - In February, Zydus Cadila signed an agreement with Apotex SA Pty. Ltd. for manufacturer of Amoxycillin, Ampicillin, Co - trimoxazole, paracetamol. - Zydus Cadila has also entered into a joint venture with Korea Green Cross Corporation, Korea, to manufacture and market recombinant Hepatitis B vaccine in India. 1999 - In April, Zydus Cadila signed an agreement with Ethical Holdings Plc, Beta Pharma, and Ethical Pharma South America S.A. for Know-how Licence Agreement to manufacture, marketing and sell transdermal pharmaceutical formulations. - In September, Zydus Cadila signed an agreement with Cherry Valley Farms Ltd., UK for supply of vaccine eggs. - Zydus Cadila has entered into a 50:50 joint venture with Byk Gulden of Germany, a renowned, research-oriented Pharma company of Germany and the world-wide patent holder of the novel proton pump inhibitor, "Pantoprazole". - During the year under report, the Company had issued 2,00,000 12% Cumulative Redeemable Preference shares of Rs. 100/- each fully paid to the members of the Company, which are redeemable at par on 1st July, 2001. - During the year under report, Indon Healthcare Limited and Zydus Aqrovet Limited, have become wholly owned subsidiaries of the company. - During the year under report, the Company has undertaken to set up a new project for manufacturing the bulk drug-Losartan at Ankleshwar. - The Company laid the foundation for a new feed supplement plant, at Vatwa. The feed supplement for poultry and cattle has been developed by tie company's R & D bio-tech department. - The Company has set up a joint venture company to manufacture the break-through molecule Pantoprazole. The Company is also undertaking discovery research projects with Byk Gulden as a pan of the Joint Venture. - The Company has entered into a technical-cum-marketing tie-up with the Swiss Serum and Vaccine Institute, Berne, Institute to launch a range of vaccines in India. - The Company has entered into a joint venture with the Haffkine institute to undertake research in the field of human vaccine and equine sera. - A new State-of-Art Research & Development centre being set-up with the capital cost of approximately Rs. 25.00 crores in the Village: Moraiya. Taluka:Sanand, Dist.: Ahmedabad. - During the year under report the Company has launched several new products in the market : Vac Typh, HB Vac, Xylodac, Losartan, Losacar was the first to be launched in India & Matergam P. - The Company has set up manufacturing premises to manufacture the feed supplement - Improval at GIDC Vatwa. - Shir Pranlal Bhogilal was appointed as an additional Director of the Company with effect from 15th December, 1998 pursuant to Section 260 of the Companies Act, 1956. - Shri Mukesh M. Patel Director of the Company retires by rotation and he is eligible for reappointment. - A new welfare policy has been introduced for employees of the Company. 2000 - The Company is setting up wholly owned subsidiaries abroad and plans to acquire overseas companies to market products. - The Company has entered into License Agreement for phased manufacture and technical know-how transfer with Swiss Serum and Vaccine Institute, Switzerland for the manufacture of Purified Cuck Embroy Vaccine. - The Country's fifth largest pharmaceutical company, is considering offering stocks to its employees through an employees' stock option scheme. - The Company has launched two drugs for the treatment of human immunodeficiency virus. - The Bulk Drugs at Ankleshwar in Gujarat has an ISO 9002 certification for the manufacture and supply of a number of molecules. - Public Issue of 1,48,86,000 No. of Equity shares ("Issue") of Rs 5/- each issued for cash at a premium of Rs [] per share aggregating Rs [] million. The Issue includes a Book Built Portion of 1,33,97,400 No. of equity shares and a Fixed price portion of 14,88,600 No. of Equity Shares. - Authorised share capital of the Company is Rs 500 million divided into 9,00,00,000 No. of Equity Shares of Rs 5/- each and 5,00,000 Preference Shares of Rs 100/- each. - During the year under report, the Company has been recognise as a "Prestigious Unit" and granted adhoc eligibility for Sales Tax deferment by the Industries Commissionerate, Gandhinagar, under New Incentive Policy - Capital Investment Incentive to Premier/ Prestigious unit scheme 1995-2000. - During the year under report Zydus Pharmaceuticals Limited and Zoom Properties Limited have become Wholly Owned Subsidiaries of the Company. - The Company has formed a JV Company in the name of Zydus Byk Healthcare Limited with an equal participation in collaboration with Byk Gulden Lomberg Chemische Fabrik GmbH, Germany, for manufacturing of Bulk Drugs, Formulations and R & D. - The Company has also formed a JV Company in the name of Sarabhai Zydus Animal Health Ltd. in collaboration with Ambalal Sarabhai Enterprises Ltd., Baroda, with an equal participation to carry on the business of animal health segments. - The company has also entered into a technical collaboration with Ethical Holdings of U.K. to manufacture and market transdermal patches in India. - The Company launched block-buster molecules Atorvastatin (Atorva), Lamivudine (Lamidac 100) and Celecoxib (Zycel), Meloxicam (Mel-OD) and Carvedilol (Carvil) during the year. - The company was the first to launch the anti-hypertensive drug Losartan in India. - Currently ranked 6th largest pharmaceutical company in India, Cadila Healthcare is one of the fastest growing pharmaceutical companies in the country. - It has also entered into a technical collaboration with Ethical Holdings of the UK to manufacture and market transdermal patches in India. - Zydus Cadilla has also entered into a technical collaboration with Ethical Holdings of the UK to manufacture and market transdermal patches in India. - Cadlia Healthcare (CHL) has signed an MoU with Rs 54 crore Recon Limited, whereby it will acquire all the 8 formulation brands of the Bangalore based comapny, as well as its distribution network. - The new company, `Recon Healthcare Ltd' is now a subsidiary of Zydus Cadila with Zydus holding 90 per cent stake. - Cadila Healthcare Ltd is setting up wholly owned subsidiaries abroad and plans to acquire overseas companies to market products. - Cadila also launched zidovudine, which is imported and marketed under the brand name Zydowin. Zidovudine, commonly called AZT, is an AIDS-retardant drug made by Glaxo Wellcome. - Zydus Alidac, the marketing arm of Cadila Healthcare Ltd., has launched www.penegra.org. -The Ahmedabad-based Cadoila Healthcare has completed the phase-III clinical trials and the bioequivalence study of the wonder drug sildenafil citrate (Viagra). 2001 - Cadila Healthcare has signed a three year collaborative R&D agreement with Danish biotech company Pantheco in the field of anti-bacterials. - The neurosciences division launched by the company has introduced anxiolytic paroxetine for the first time in the country. - Cadila Healthcare Ltd has posted a 14.75 per cent increase in net profit at Rs 21.86 crore for the quarter ended September 30, 2001. 2002 -Cadila Healthcare Ltd has informed BSE that at the meeting of the Board of Directors of the company held on August 20, 2002 it has been decided to issue/allot Secured Redeemable Non Convertible Debentures for an aggregate face value of Rs 700 million by private placement basis at an interest rate of 8.40% p.a. 2003 -Mr.UpenShah has been designated as the Company Secretary and Compliance Officer of Cadila Healthcare Ltd. -Zydus Cadila, the ahmedabad based healthcare has bagged global marketing rights of an anti-rabies vaccine of vaxirab a swiss company Berna Biotech. -Cadila Healthcare receives Mumbai High court approval for the scheme of amalgamation with German Remedies Ltd and Zoom Properties Ltd. -Cadila Healthcare Ltd has acquired US base Alpharma Inc's French Subsidiary Alpharma SAS France for a consideration of Euro 5.5 million. -Mr.H.K.Bilpodiwala, Mr.H.Dhanarajgir and Mr.A.S Diwanji have been appointed as the additional directors on the board of the company. -Zydus Cadila Healthcare Ltd has signed a pact with Schering AG, Germany which allows the Indian Pharmaceuticals major to market Schering's patented products in India. -Duphar Interfran, a subsidiary of Fermenta Biotech Ltd signed an agreement with Cadila Ltd for the sale of FBL's global patents of Chiral Building blocks and process teechnology for the manufacture of Lisinopril and Benazepril. -Zydus forges marketing pact with Schering 2004 -Zydus Cadila sets up Zydus Pharmaceuticals USA, Inc -Zydus Cadila inks strategic pact with Boehringer Ingelheim -Zyndus Altana Healthcare - the JV between Altana Pharma AG and Zyndus Cadila, has been accredited with the ISO 9001-2000 certificate. 2005 - Zydus Cadila receives approval from the USFDA to market the anti-hypertensive drug, Atenolol, and an anti-infective drug, Clindamycin on 31 Jan and 1 Feb. -Zydus Cadila unveils 'Pitavastatin' to control cholesterol on February 21, 2005 -Cadila ties up with Tyco unit to sell generic drugs in US - Launches NuPatch - India's first indigenously manufactured Diclofenac transdermal patch for pain relief. -Cadila Healthcare & Mayne signs agreement to set up JVC to manufacture specialty oncology products -Cadila Healthcare - German Remedies launches Fludara Oral for Lymphocytic Leukaemia -Zydus Cadila receives tentative approval for Divalproex Sodium DR Tablets from US FDA -Cadila Healthcare receives approval for Promethazine Tablets from USFDA -Cadila Healthcare enters into JV with BSVL 2006 -Zydus Cadila forges alliance with French firm -Zydus Cadila receives USFDA approval for Simvastatin Tablets -Zydus Cadila to acquire Nutralite - India's largest selling cholesterol-free margarine -Sarabhai Zydus to roll out immuno-diagnostics kits -Cadila Healthcare has given the Bonus in the Ratio of 1:1 2007 -Cadila Healthcare Ltd on April 19, 2007 has announced the acquisition of Nippon Universal Pharmaceutical Ltd. - Cadila Healthcare Ltd has announced that its second overseas acquisition this year, the Company signed an agreement to acquire 100% stake in Quimica e Farmaceutica Nikkho do Brasil Ltda. -Zydus Cadila acquires Nippon Universal, strengthens its presence in Japan -Zydus Cadila, the first to launch revolutionary anti-obesity drug Slimona in India -Zydus Cadila acquires Brazilian Company Nikkho 2008 -Zylus Cadila, Karo Bio to jointly develop new drugs -Zydus Cadila & Karo Bio of Sweden sign research agreement for a novel drug to treat inflammatory diseases -Zydus Cadila acquires Etna Biotech, a subsidiary of Crucell N.V. -Zydus scores with first day launch of Venlafaxine Hydrochloride in the US 2009 -Zydus Cadila announces research collaboration to discover and develop new cardiovascular medicines -Zydus Research Centre Receives AAALAC Accreditation 2010 -CHL announces Bonus Shares in the ratio of 1:2 - India unveiled its first indigenous H1N1 vaccine, which was developed by drug firm Cadila Healthcare and this vaccine will provide immunity from the H1N1 virus strain for one year. 2011 -Company has signed an Agreement with Bayer HealthCare to set up 50:50 Joint Venture Company in the name of "Bayer Zydus Pharma -Cadila gets USFDA nod for diabetes drug trial -Cadila Health acquires Bremer Pharma from ICICI Venture 2012 -"Cadila Healthcare enters into a settlement and license agreement with Somaxon for Silenor" -Cadila Healthcare gets USFDA nod for Aripiprazole orally disintegrating tablets 2013 -Zydus Cadila receives tentative approval for Doxepin Hcl tablets -Zydus and IDRI sign agreement for the development of IDRI's Vaccine Candidate for Visceral Leishmaniasis (Kala-Azar) -Zydus and Pieris Sign Broad Co-Development Alliance for Novel Anticalinr Therapeutics -Zydus Pharmaceuticals (USA) Inc agreement with Warner Chilcott Company LLC 2014 -Zydus and gilead enter into a generic licensing agreement to manufacture breakthrough treatment for hepatitis c -Zydus launches world's first biosimilar of Adalimumab -Cadila Healthcar - Lipaglyn - India's first NCE launched in the market -Zydus and IDRI sign agreement for the development of IDRI's -Zydus and Pieris Sign Broad Co-Development Alliance for Novel 2015 -Zydus Cadila has completed the single ascending dose (SAD) range -Zydus launches SoviHep - the breakthrough therapy for Hepatitis C in alliance with Gilead Sciences -Cadila Healthcare Ltd has purchased the remaining 50 per cent shares of its joint venture firm, Zydus BSV Pharma Pvt Ltd (Zydus BSV) -Cadila Healthcare Ltd has received the final approval from USFDA for Pyridostigmine Bromide Tablets -Cadila Healthcare Ltd has received the market authorisation from the United States Food and Drug Administration to market drug for the treatment of chronic pain or cancer related pain. -Cadila Healthcare Ltd has received final approval from the USFDA to market Amiloride Hydrochloride Tablets USP, 5 mg -Zydus launches 'Tenglyn', the most affordable gliptin for diabetics in India -Cadila Healthcare has splits its face value from Rs. 5 to Rs. 1 2016 -Zydus Cadila acquires select animal health brands of Zoetis -Cadila Healthcar - Zydus receives final approval from the USFDA for Glyburide and Metformin Hcl Tablets USP -Cadila Healthcar - Zydus acquires the gastro therapy 'Actibile' from Albert David Limited -Zydus gets USFDA approval for Glyburide Tablets -Cadila Healthcar - Zydus acquires two ANDAs from Teva, strengthens its US portfolio -Cadila Healthcar - Zydus acquires six brands from MSD 2017 -Zydus receives final approval from the USFDA for Temozolomide Capsules and Nadolol Tablets USP. - 'Zydus Cadila acquires Sentynl Therapeutics Inc., a US based specialty pharmaceutical company'. -Zydus and Pharm Aid Ltd., enter into an exclusive agreement for vaccine technology in Russia. -Zydus receives EIR Report for Manufacturing Facility at the Pharma SEZ at Ahmedabad. -Zydus receives final approval from the USFDA for Desvenlafaxine Extended-Release Tablets. -Cadila Healthcare enters into agreement with Phibro Animal Health Corporation to license Phibro innovative poultry vaccine technologies and know-how to a new vaccine manufacturing facility to be built by Zydus Cadila to serve the fast growing poultry market in India. 2018 -Zydus Cadila gets USFDA nod for sedative injection. -Zydus enters into agreement with Medicure International to commercialize New Drug Application (NDA) product, pitavastatin magnesium (ZYPITAMAG TM ) in the United States. -Zydus Cadila bags approval from the USFDA to market Omeprazole and Sodium Bicarbonate Capsules 20 mg/1100 mg (OTC). -Zydus Cadila bags approval for Carbidopa Tablets. -CSIR-IMTECH inks pact with Zydus Cadila. -Zydus Cadila launches generic erectile dysfunction drug in US. 2019 -Zydus launches Ramelteon Tablets for treatment of insomnia. -Zydus receives tentative USFDA approval for Lorcaserin Hydrochloride Tablets used in the treatment of obesity. 2020 -Zydus & CMS enter pact for Desidustat in Greater China. -Zydus Wellness launches hand sanitizer under Nycil brand to meet growing demand. -Zydus Cadila launches COVID-19 drug Remdesivir in India. -Zydus Cadila launches new product for COPD patients in India. 2021 -Zydus Cadila launches Trastuzumab Emtansine under brand name Ujvira. -Cadila Healthcare receives orphan drug designation for malaria treatment compound. 2022 -Zydus Life gets USFDA final approvals for Silodosin, Pregabalin. -Zydus Group had 338 approvals and filed over 431 ANDAs since the commencement of the filing process -Zydus Life gets final USFDA approval for Topiramate extended-release capsules. -Zydus Lifesciences' arm gets EC nod for MoCD injection. -Pharma Company Of The Year Award by ETHealthworld India Pharmaworld Awards 2022. -Excellence In CSR at ETHealthworld India Pharmaworld Awards 2022. -7th India Pharma and India Medical Device award by the Government of India, Department of Pharmaceuticals in the India Pharma CSR of the year category. 2023 -Zydus Lifesciences inks licensing pact with Daewoong Pharmaceutical. -Zydus Lifesciences receives USFDA approval for Acyclovir Cream. -""Sentynl Therapeutics Completes Asset Transfer of CUTX-101 Copper Histidinate Product Candidate for Treatment of Menkes Disease from Cyprium Therapeutics"". -Zydus lifesciences limited received 7th CSR Health Impact Award under CSR Health Project (Large Corporate) 2023 by IHW Council for our Healthcare Project in aspiration district. 2024 -Zydus Lifesciences gets WHO prequalification for Typhoid Vi conjugate vaccine. - Zydus Lifesciences gets Mexican regulatory nod for cancer treatment biosimilar.

1995 - The Company was incorporated as Cadila Healthcare Private Ltd. on May 15, under the company act, 1956 and subsequently the Company was converted into a public company and then renamed as Cadila Healthcare Ltd. effective from Juy 17, 1996. - The name "Cadila" shall be used only for "Cadila Healthcare Limited" (Zydus Cadila), "Cadila Pharmaceuticals Limited" (CPL) and "Cadila Laboratories Limited" (CLL). - The Company is flagship company of Zydus Cadila Group. - The Company's operations include pharmaceuticals (human formulations, veterinary formulations and bulk drugs); diagnostics, herbal products, skin care products and other OTC products. - The Company has 6 subsidiaries Indon Healthcare Ltd., Zydus Pharmaceuticals Ltd., Zudus Aqrovet Ltd., Zoom Properties Pvt. Ltd., Zydus International Pvt. Ltd., Ireland and Zydus Healthcare S.A. (Pvt) Ltd., South Africa. - Zydus Cadila signed an agreement with Anda Biologicals, France, for Marketing and distribution of diagnostic kits. Anda to appoint a max. of two distributors in India. 1996 - Zydus Cadila signed an agreement with Centeon L.L.C., USA and Centeon Pharama GMBH, Germany for Exclusive rights to sell and distribute plasma products in India and Nepal. - In May, Zydus Cadila signed an agreement with Acta Services Srl., Rome for distribution of Diagnostic instrument Acto 1 Analyser manu. By Acta. - In June, Zydus Cadila signed an agreement with China Resources Gulin Pharma, Works, China, for exclusive supply of Artesunate Granules to Zydus Cadila. - In July, Zydus Cadila signed an agreement with Shimizu Chemical Corporation, Japan, for Marketing of specified products by Zydus Cadila in India. 1997 - A Scheme of Arrangement and Amalgamation was sanctioned by honorable High Court of Gujarat by order passed on May 2 issued on August 16th. - Zydus Cadila would issued 1,48,423 fully paid-up equity shares of Rs 10/- each to the shareholders of Patel Group in exchange for the assets transferred to them of Transferor companies. - Zydus Cadila has also tied-up with Regional Research Laboratory Jammu, to develop Enzymatic Resolution for Paroxetine HCL and some other Enzymatic products. 1998 - In February, Zydus Cadila signed an agreement with Apotex SA Pty. Ltd. for manufacturer of Amoxycillin, Ampicillin, Co - trimoxazole, paracetamol. - Zydus Cadila has also entered into a joint venture with Korea Green Cross Corporation, Korea, to manufacture and market recombinant Hepatitis B vaccine in India. 1999 - In April, Zydus Cadila signed an agreement with Ethical Holdings Plc, Beta Pharma, and Ethical Pharma South America S.A. for Know-how Licence Agreement to manufacture, marketing and sell transdermal pharmaceutical formulations. - In September, Zydus Cadila signed an agreement with Cherry Valley Farms Ltd., UK for supply of vaccine eggs. - Zydus Cadila has entered into a 50:50 joint venture with Byk Gulden of Germany, a renowned, research-oriented Pharma company of Germany and the world-wide patent holder of the novel proton pump inhibitor, "Pantoprazole". - During the year under report, the Company had issued 2,00,000 12% Cumulative Redeemable Preference shares of Rs. 100/- each fully paid to the members of the Company, which are redeemable at par on 1st July, 2001. - During the year under report, Indon Healthcare Limited and Zydus Aqrovet Limited, have become wholly owned subsidiaries of the company. - During the year under report, the Company has undertaken to set up a new project for manufacturing the bulk drug-Losartan at Ankleshwar. - The Company laid the foundation for a new feed supplement plant, at Vatwa. The feed supplement for poultry and cattle has been developed by tie company's R & D bio-tech department. - The Company has set up a joint venture company to manufacture the break-through molecule Pantoprazole. The Company is also undertaking discovery research projects with Byk Gulden as a pan of the Joint Venture. - The Company has entered into a technical-cum-marketing tie-up with the Swiss Serum and Vaccine Institute, Berne, Institute to launch a range of vaccines in India. - The Company has entered into a joint venture with the Haffkine institute to undertake research in the field of human vaccine and equine sera. - A new State-of-Art Research & Development centre being set-up with the capital cost of approximately Rs. 25.00 crores in the Village: Moraiya. Taluka:Sanand, Dist.: Ahmedabad. - During the year under report the Company has launched several new products in the market : Vac Typh, HB Vac, Xylodac, Losartan, Losacar was the first to be launched in India & Matergam P. - The Company has set up manufacturing premises to manufacture the feed supplement - Improval at GIDC Vatwa. - Shir Pranlal Bhogilal was appointed as an additional Director of the Company with effect from 15th December, 1998 pursuant to Section 260 of the Companies Act, 1956. - Shri Mukesh M. Patel Director of the Company retires by rotation and he is eligible for reappointment. - A new welfare policy has been introduced for employees of the Company. 2000 - The Company is setting up wholly owned subsidiaries abroad and plans to acquire overseas companies to market products. - The Company has entered into License Agreement for phased manufacture and technical know-how transfer with Swiss Serum and Vaccine Institute, Switzerland for the manufacture of Purified Cuck Embroy Vaccine. - The Country's fifth largest pharmaceutical company, is considering offering stocks to its employees through an employees' stock option scheme. - The Company has launched two drugs for the treatment of human immunodeficiency virus. - The Bulk Drugs at Ankleshwar in Gujarat has an ISO 9002 certification for the manufacture and supply of a number of molecules. - Public Issue of 1,48,86,000 No. of Equity shares ("Issue") of Rs 5/- each issued for cash at a premium of Rs [] per share aggregating Rs [] million. The Issue includes a Book Built Portion of 1,33,97,400 No. of equity shares and a Fixed price portion of 14,88,600 No. of Equity Shares. - Authorised share capital of the Company is Rs 500 million divided into 9,00,00,000 No. of Equity Shares of Rs 5/- each and 5,00,000 Preference Shares of Rs 100/- each. - During the year under report, the Company has been recognise as a "Prestigious Unit" and granted adhoc eligibility for Sales Tax deferment by the Industries Commissionerate, Gandhinagar, under New Incentive Policy - Capital Investment Incentive to Premier/ Prestigious unit scheme 1995-2000. - During the year under report Zydus Pharmaceuticals Limited and Zoom Properties Limited have become Wholly Owned Subsidiaries of the Company. - The Company has formed a JV Company in the name of Zydus Byk Healthcare Limited with an equal participation in collaboration with Byk Gulden Lomberg Chemische Fabrik GmbH, Germany, for manufacturing of Bulk Drugs, Formulations and R & D. - The Company has also formed a JV Company in the name of Sarabhai Zydus Animal Health Ltd. in collaboration with Ambalal Sarabhai Enterprises Ltd., Baroda, with an equal participation to carry on the business of animal health segments. - The company has also entered into a technical collaboration with Ethical Holdings of U.K. to manufacture and market transdermal patches in India. - The Company launched block-buster molecules Atorvastatin (Atorva), Lamivudine (Lamidac 100) and Celecoxib (Zycel), Meloxicam (Mel-OD) and Carvedilol (Carvil) during the year. - The company was the first to launch the anti-hypertensive drug Losartan in India. - Currently ranked 6th largest pharmaceutical company in India, Cadila Healthcare is one of the fastest growing pharmaceutical companies in the country. - It has also entered into a technical collaboration with Ethical Holdings of the UK to manufacture and market transdermal patches in India. - Zydus Cadilla has also entered into a technical collaboration with Ethical Holdings of the UK to manufacture and market transdermal patches in India. - Cadlia Healthcare (CHL) has signed an MoU with Rs 54 crore Recon Limited, whereby it will acquire all the 8 formulation brands of the Bangalore based comapny, as well as its distribution network. - The new company, `Recon Healthcare Ltd' is now a subsidiary of Zydus Cadila with Zydus holding 90 per cent stake. - Cadila Healthcare Ltd is setting up wholly owned subsidiaries abroad and plans to acquire overseas companies to market products. - Cadila also launched zidovudine, which is imported and marketed under the brand name Zydowin. Zidovudine, commonly called AZT, is an AIDS-retardant drug made by Glaxo Wellcome. - Zydus Alidac, the marketing arm of Cadila Healthcare Ltd., has launched www.penegra.org. -The Ahmedabad-based Cadoila Healthcare has completed the phase-III clinical trials and the bioequivalence study of the wonder drug sildenafil citrate (Viagra). 2001 - Cadila Healthcare has signed a three year collaborative R&D agreement with Danish biotech company Pantheco in the field of anti-bacterials. - The neurosciences division launched by the company has introduced anxiolytic paroxetine for the first time in the country. - Cadila Healthcare Ltd has posted a 14.75 per cent increase in net profit at Rs 21.86 crore for the quarter ended September 30, 2001.YEAR EVENTS 1995 - The Company was incorporated as Cadila Healthcare Private Ltd. on May 15, under the company act, 1956 and subsequently the Company was converted into a public company and then renamed as Cadila Healthcare Ltd. effective from Juy 17, 1996. - The name "Cadila" shall be used only for "Cadila Healthcare Limited" (Zydus Cadila), "Cadila Pharmaceuticals Limited" (CPL) and "Cadila Laboratories Limited" (CLL). - The Company is flagship company of Zydus Cadila Group. - The Company's operations include pharmaceuticals (human formulations, veterinary formulations and bulk drugs); diagnostics, herbal products, skin care products and other OTC products. - The Company has 6 subsidiaries Indon Healthcare Ltd., Zydus Pharmaceuticals Ltd., Zudus Aqrovet Ltd., Zoom Properties Pvt. Ltd., Zydus International Pvt. Ltd., Ireland and Zydus Healthcare S.A. (Pvt) Ltd., South Africa. - Zydus Cadila signed an agreement with Anda Biologicals, France, for Marketing and distribution of diagnostic kits. Anda to appoint a max. of two distributors in India. 1996 - Zydus Cadila signed an agreement with Centeon L.L.C., USA and Centeon Pharama GMBH, Germany for Exclusive rights to sell and distribute plasma products in India and Nepal. - In May, Zydus Cadila signed an agreement with Acta Services Srl., Rome for distribution of Diagnostic instrument Acto 1 Analyser manu. By Acta. - In June, Zydus Cadila signed an agreement with China Resources Gulin Pharma, Works, China, for exclusive supply of Artesunate Granules to Zydus Cadila. - In July, Zydus Cadila signed an agreement with Shimizu Chemical Corporation, Japan, for Marketing of specified products by Zydus Cadila in India. 1997 - A Scheme of Arrangement and Amalgamation was sanctioned by honorable High Court of Gujarat by order passed on May 2 issued on August 16th. - Zydus Cadila would issued 1,48,423 fully paid-up equity shares of Rs 10/- each to the shareholders of Patel Group in exchange for the assets transferred to them of Transferor companies. - Zydus Cadila has also tied-up with Regional Research Laboratory Jammu, to develop Enzymatic Resolution for Paroxetine HCL and some other Enzymatic products. 1998 - In February, Zydus Cadila signed an agreement with Apotex SA Pty. Ltd. for manufacturer of Amoxycillin, Ampicillin, Co - trimoxazole, paracetamol. - Zydus Cadila has also entered into a joint venture with Korea Green Cross Corporation, Korea, to manufacture and market recombinant Hepatitis B vaccine in India. 1999 - In April, Zydus Cadila signed an agreement with Ethical Holdings Plc, Beta Pharma, and Ethical Pharma South America S.A. for Know-how Licence Agreement to manufacture, marketing and sell transdermal pharmaceutical formulations. - In September, Zydus Cadila signed an agreement with Cherry Valley Farms Ltd., UK for supply of vaccine eggs. - Zydus Cadila has entered into a 50:50 joint venture with Byk Gulden of Germany, a renowned, research-oriented Pharma company of Germany and the world-wide patent holder of the novel proton pump inhibitor, "Pantoprazole". - During the year under report, the Company had issued 2,00,000 12% Cumulative Redeemable Preference shares of Rs. 100/- each fully paid to the members of the Company, which are redeemable at par on 1st July, 2001. - During the year under report, Indon Healthcare Limited and Zydus Aqrovet Limited, have become wholly owned subsidiaries of the company. - During the year under report, the Company has undertaken to set up a new project for manufacturing the bulk drug-Losartan at Ankleshwar. - The Company laid the foundation for a new feed supplement plant, at Vatwa. The feed supplement for poultry and cattle has been developed by tie company's R & D bio-tech department. - The Company has set up a joint venture company to manufacture the break-through molecule Pantoprazole. The Company is also undertaking discovery research projects with Byk Gulden as a pan of the Joint Venture. - The Company has entered into a technical-cum-marketing tie-up with the Swiss Serum and Vaccine Institute, Berne, Institute to launch a range of vaccines in India. - The Company has entered into a joint venture with the Haffkine institute to undertake research in the field of human vaccine and equine sera. - A new State-of-Art Research & Development centre being set-up with the capital cost of approximately Rs. 25.00 crores in the Village: Moraiya. Taluka:Sanand, Dist.: Ahmedabad. - During the year under report the Company has launched several new products in the market : Vac Typh, HB Vac, Xylodac, Losartan, Losacar was the first to be launched in India & Matergam P. - The Company has set up manufacturing premises to manufacture the feed supplement - Improval at GIDC Vatwa. - Shir Pranlal Bhogilal was appointed as an additional Director of the Company with effect from 15th December, 1998 pursuant to Section 260 of the Companies Act, 1956. - Shri Mukesh M. Patel Director of the Company retires by rotation and he is eligible for reappointment. - A new welfare policy has been introduced for employees of the Company. 2000 - The Company is setting up wholly owned subsidiaries abroad and plans to acquire overseas companies to market products. - The Company has entered into License Agreement for phased manufacture and technical know-how transfer with Swiss Serum and Vaccine Institute, Switzerland for the manufacture of Purified Cuck Embroy Vaccine. - The Country's fifth largest pharmaceutical company, is considering offering stocks to its employees through an employees' stock option scheme. - The Company has launched two drugs for the treatment of human immunodeficiency virus. - The Bulk Drugs at Ankleshwar in Gujarat has an ISO 9002 certification for the manufacture and supply of a number of molecules. - Public Issue of 1,48,86,000 No. of Equity shares ("Issue") of Rs 5/- each issued for cash at a premium of Rs [] per share aggregating Rs [] million. The Issue includes a Book Built Portion of 1,33,97,400 No. of equity shares and a Fixed price portion of 14,88,600 No. of Equity Shares. - Authorised share capital of the Company is Rs 500 million divided into 9,00,00,000 No. of Equity Shares of Rs 5/- each and 5,00,000 Preference Shares of Rs 100/- each. - During the year under report, the Company has been recognise as a "Prestigious Unit" and granted adhoc eligibility for Sales Tax deferment by the Industries Commissionerate, Gandhinagar, under New Incentive Policy - Capital Investment Incentive to Premier/ Prestigious unit scheme 1995-2000. - During the year under report Zydus Pharmaceuticals Limited and Zoom Properties Limited have become Wholly Owned Subsidiaries of the Company. - The Company has formed a JV Company in the name of Zydus Byk Healthcare Limited with an equal participation in collaboration with Byk Gulden Lomberg Chemische Fabrik GmbH, Germany, for manufacturing of Bulk Drugs, Formulations and R & D. - The Company has also formed a JV Company in the name of Sarabhai Zydus Animal Health Ltd. in collaboration with Ambalal Sarabhai Enterprises Ltd., Baroda, with an equal participation to carry on the business of animal health segments. - The company has also entered into a technical collaboration with Ethical Holdings of U.K. to manufacture and market transdermal patches in India. - The Company launched block-buster molecules Atorvastatin (Atorva), Lamivudine (Lamidac 100) and Celecoxib (Zycel), Meloxicam (Mel-OD) and Carvedilol (Carvil) during the year. - The company was the first to launch the anti-hypertensive drug Losartan in India. - Currently ranked 6th largest pharmaceutical company in India, Cadila Healthcare is one of the fastest growing pharmaceutical companies in the country. - It has also entered into a technical collaboration with Ethical Holdings of the UK to manufacture and market transdermal patches in India. - Zydus Cadilla has also entered into a technical collaboration with Ethical Holdings of the UK to manufacture and market transdermal patches in India. - Cadlia Healthcare (CHL) has signed an MoU with Rs 54 crore Recon Limited, whereby it will acquire all the 8 formulation brands of the Bangalore based comapny, as well as its distribution network. - The new company, `Recon Healthcare Ltd' is now a subsidiary of Zydus Cadila with Zydus holding 90 per cent stake. - Cadila Healthcare Ltd is setting up wholly owned subsidiaries abroad and plans to acquire overseas companies to market products. - Cadila also launched zidovudine, which is imported and marketed under the brand name Zydowin. Zidovudine, commonly called AZT, is an AIDS-retardant drug made by Glaxo Wellcome. - Zydus Alidac, the marketing arm of Cadila Healthcare Ltd., has launched www.penegra.org. -The Ahmedabad-based Cadoila Healthcare has completed the phase-III clinical trials and the bioequivalence study of the wonder drug sildenafil citrate (Viagra). 2001 - Cadila Healthcare has signed a three year collaborative R&D agreement with Danish biotech company Pantheco in the field of anti-bacterials. - The neurosciences division launched by the company has introduced anxiolytic paroxetine for the first time in the country. - Cadila Healthcare Ltd has posted a 14.75 per cent increase in net profit at Rs 21.86 crore for the quarter ended September 30, 2001. 2002 -Cadila Healthcare Ltd has informed BSE that at the meeting of the Board of Directors of the company held on August 20, 2002 it has been decided to issue/allot Secured Redeemable Non Convertible Debentures for an aggregate face value of Rs 700 million by private placement basis at an interest rate of 8.40% p.a. 2003 -Mr.UpenShah has been designated as the Company Secretary and Compliance Officer of Cadila Healthcare Ltd. -Zydus Cadila, the ahmedabad based healthcare has bagged global marketing rights of an anti-rabies vaccine of vaxirab a swiss company Berna Biotech. -Cadila Healthcare receives Mumbai High court approval for the scheme of amalgamation with German Remedies Ltd and Zoom Properties Ltd. -Cadila Healthcare Ltd has acquired US base Alpharma Inc's French Subsidiary Alpharma SAS France for a consideration of Euro 5.5 million. -Mr.H.K.Bilpodiwala, Mr.H.Dhanarajgir and Mr.A.S Diwanji have been appointed as the additional directors on the board of the company. -Zydus Cadila Healthcare Ltd has signed a pact with Schering AG, Germany which allows the Indian Pharmaceuticals major to market Schering's patented products in India. -Duphar Interfran, a subsidiary of Fermenta Biotech Ltd signed an agreement with Cadila Ltd for the sale of FBL's global patents of Chiral Building blocks and process teechnology for the manufacture of Lisinopril and Benazepril. -Zydus forges marketing pact with Schering 2004 -Zydus Cadila sets up Zydus Pharmaceuticals USA, Inc -Zydus Cadila inks strategic pact with Boehringer Ingelheim -Zyndus Altana Healthcare - the JV between Altana Pharma AG and Zyndus Cadila, has been accredited with the ISO 9001-2000 certificate. 2005 - Zydus Cadila receives approval from the USFDA to market the anti-hypertensive drug, Atenolol, and an anti-infective drug, Clindamycin on 31 Jan and 1 Feb. -Zydus Cadila unveils 'Pitavastatin' to control cholesterol on February 21, 2005 -Cadila ties up with Tyco unit to sell generic drugs in US - Launches NuPatch - India's first indigenously manufactured Diclofenac transdermal patch for pain relief. -Cadila Healthcare & Mayne signs agreement to set up JVC to manufacture specialty oncology products -Cadila Healthcare - German Remedies launches Fludara Oral for Lymphocytic Leukaemia -Zydus Cadila receives tentative approval for Divalproex Sodium DR Tablets from US FDA -Cadila Healthcare receives approval for Promethazine Tablets from USFDA -Cadila Healthcare enters into JV with BSVL 2006 -Zydus Cadila forges alliance with French firm -Zydus Cadila receives USFDA approval for Simvastatin Tablets -Zydus Cadila to acquire Nutralite - India's largest selling cholesterol-free margarine -Sarabhai Zydus to roll out immuno-diagnostics kits -Cadila Healthcare has given the Bonus in the Ratio of 1:1 2007 -Cadila Healthcare Ltd on April 19, 2007 has announced the acquisition of Nippon Universal Pharmaceutical Ltd. - Cadila Healthcare Ltd has announced that its second overseas acquisition this year, the Company signed an agreement to acquire 100% stake in Quimica e Farmaceutica Nikkho do Brasil Ltda. -Zydus Cadila acquires Nippon Universal, strengthens its presence in Japan -Zydus Cadila, the first to launch revolutionary anti-obesity drug Slimona in India -Zydus Cadila acquires Brazilian Company Nikkho 2008 -Zylus Cadila, Karo Bio to jointly develop new drugs -Zydus Cadila & Karo Bio of Sweden sign research agreement for a novel drug to treat inflammatory diseases -Zydus Cadila acquires Etna Biotech, a subsidiary of Crucell N.V. -Zydus scores with first day launch of Venlafaxine Hydrochloride in the US 2009 -Zydus Cadila announces research collaboration to discover and develop new cardiovascular medicines -Zydus Research Centre Receives AAALAC Accreditation 2010 -CHL announces Bonus Shares in the ratio of 1:2 - India unveiled its first indigenous H1N1 vaccine, which was developed by drug firm Cadila Healthcare and this vaccine will provide immunity from the H1N1 virus strain for one year. 2011 -Company has signed an Agreement with Bayer HealthCare to set up 50:50 Joint Venture Company in the name of "Bayer Zydus Pharma -Cadila gets USFDA nod for diabetes drug trial -Cadila Health acquires Bremer Pharma from ICICI Venture 2012 -"Cadila Healthcare enters into a settlement and license agreement with Somaxon for Silenor" -Cadila Healthcare gets USFDA nod for Aripiprazole orally disintegrating tablets 2013 -Zydus Cadila receives tentative approval for Doxepin Hcl tablets -Zydus and IDRI sign agreement for the development of IDRI's Vaccine Candidate for Visceral Leishmaniasis (Kala-Azar) -Zydus and Pieris Sign Broad Co-Development Alliance for Novel Anticalinr Therapeutics -Zydus Pharmaceuticals (USA) Inc agreement with Warner Chilcott Company LLC 2014 -Zydus and gilead enter into a generic licensing agreement to manufacture breakthrough treatment for hepatitis c -Zydus launches world's first biosimilar of Adalimumab -Cadila Healthcar - Lipaglyn - India's first NCE launched in the market -Zydus and IDRI sign agreement for the development of IDRI's -Zydus and Pieris Sign Broad Co-Development Alliance for Novel 2015 -Zydus Cadila has completed the single ascending dose (SAD) range -Zydus launches SoviHep - the breakthrough therapy for Hepatitis C in alliance with Gilead Sciences -Cadila Healthcare Ltd has purchased the remaining 50 per cent shares of its joint venture firm, Zydus BSV Pharma Pvt Ltd (Zydus BSV) -Cadila Healthcare Ltd has received the final approval from USFDA for Pyridostigmine Bromide Tablets -Cadila Healthcare Ltd has received the market authorisation from the United States Food and Drug Administration to market drug for the treatment of chronic pain or cancer related pain. -Cadila Healthcare Ltd has received final approval from the USFDA to market Amiloride Hydrochloride Tablets USP, 5 mg -Zydus launches 'Tenglyn', the most affordable gliptin for diabetics in India -Cadila Healthcare has splits its face value from Rs. 5 to Rs. 1 2016 -Zydus Cadila acquires select animal health brands of Zoetis -Cadila Healthcar - Zydus receives final approval from the USFDA for Glyburide and Metformin Hcl Tablets USP -Cadila Healthcar - Zydus acquires the gastro therapy 'Actibile' from Albert David Limited -Zydus gets USFDA approval for Glyburide Tablets -Cadila Healthcar - Zydus acquires two ANDAs from Teva, strengthens its US portfolio -Cadila Healthcar - Zydus acquires six brands from MSD 2017 -Zydus receives final approval from the USFDA for Temozolomide Capsules and Nadolol Tablets USP. - 'Zydus Cadila acquires Sentynl Therapeutics Inc., a US based specialty pharmaceutical company'. -Zydus and Pharm Aid Ltd., enter into an exclusive agreement for vaccine technology in Russia. -Zydus receives EIR Report for Manufacturing Facility at the Pharma SEZ at Ahmedabad. -Zydus receives final approval from the USFDA for Desvenlafaxine Extended-Release Tablets. -Cadila Healthcare enters into agreement with Phibro Animal Health Corporation to license Phibro innovative poultry vaccine technologies and know-how to a new vaccine manufacturing facility to be built by Zydus Cadila to serve the fast growing poultry market in India. 2018 -Zydus Cadila gets USFDA nod for sedative injection. -Zydus enters into agreement with Medicure International to commercialize New Drug Application (NDA) product, pitavastatin magnesium (ZYPITAMAG TM ) in the United States. -Zydus Cadila bags approval from the USFDA to market Omeprazole and Sodium Bicarbonate Capsules 20 mg/1100 mg (OTC). -Zydus Cadila bags approval for Carbidopa Tablets. -CSIR-IMTECH inks pact with Zydus Cadila. -Zydus Cadila launches generic erectile dysfunction drug in US. 2019 -Zydus launches Ramelteon Tablets for treatment of insomnia. -Zydus receives tentative USFDA approval for Lorcaserin Hydrochloride Tablets used in the treatment of obesity. 2020 -Zydus & CMS enter pact for Desidustat in Greater China. -Zydus Wellness launches hand sanitizer under Nycil brand to meet growing demand. -Zydus Cadila launches COVID-19 drug Remdesivir in India. -Zydus Cadila launches new product for COPD patients in India. 2021 -Zydus Cadila launches Trastuzumab Emtansine under brand name Ujvira. -Cadila Healthcare receives orphan drug designation for malaria treatment compound. 2022 -Zydus Life gets USFDA final approvals for Silodosin, Pregabalin. -Zydus Group had 338 approvals and filed over 431 ANDAs since the commencement of the filing process -Zydus Life gets final USFDA approval for Topiramate extended-release capsules. -Zydus Lifesciences' arm gets EC nod for MoCD injection. -Pharma Company Of The Year Award by ETHealthworld India Pharmaworld Awards 2022. -Excellence In CSR at ETHealthworld India Pharmaworld Awards 2022. -7th India Pharma and India Medical Device award by the Government of India, Department of Pharmaceuticals in the India Pharma CSR of the year category. 2023 -Zydus Lifesciences inks licensing pact with Daewoong Pharmaceutical. -Zydus Lifesciences receives USFDA approval for Acyclovir Cream. -""Sentynl Therapeutics Completes Asset Transfer of CUTX-101 Copper Histidinate Product Candidate for Treatment of Menkes Disease from Cyprium Therapeutics"". -Zydus lifesciences limited received 7th CSR Health Impact Award under CSR Health Project (Large Corporate) 2023 by IHW Council for our Healthcare Project in aspiration district. 2024 -Zydus Lifesciences gets WHO prequalification for Typhoid Vi conjugate vaccine. - Zydus Lifesciences gets Mexican regulatory nod for cancer treatment biosimilar.

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Parent Organisation

Zydus Lifesciences Ltd.

Founded

15/05/1995

Managing Director

Dr.Sharvil P Patel

NSE Symbol

ZYDUSLIFEEQ

FAQ

The current price of Zydus Lifesciences Ltd is ₹ 888.05.

The 52-week high for Zydus Lifesciences Ltd is ₹ 894.85 and the 52-week low is ₹ 877.05.

The market capitalization of Zydus Lifesciences Ltd is currently ₹ 89358.61. This value can fluctuate based on stock price movements and changes in the number of shares outstanding.

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The CEO of Zydus Lifesciences Ltd is Dr.Sharvil P Patel, who has been leading the company with a vision to expand its renewable energy portfolio and drive sustainable growth.

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