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Chairman H F Khorakiwala
Independent Director Aman Mehta
Managing Director Murtaza H Khorakiwala
Director Huzaifa H Khorakiwala
Independent Director Sanjaya Baru
Independent Director D S Brar
Independent Director Tasneem Mehta
Independent Director B R Arora
Company Secretary Narendra Singh
Independent Director Vinesh Kumar Jairath
Director Zahabiya Khorakiwala
Nominee (EXIM) Rima Marphatia

Wockhardt Ltd is a global pharmaceutical and biotechnology organization, providing affordable, high-quality medicines for a healthier world. The company is Indias leading research-based global healthcare enterprise with relevance in the fields of Pharmaceuticals, Biotechnology and a chain of advanced Super Speciality Hospitals. The company has twelve manufacturing locations and there are three locations where research and development activities are carried out.Wockhardt has manufacturing and research facilities in India, USA & UK and a manufacturing facility in Ireland. Wockhardt has a significant presence in USA, Europe and India, with 61% of its global revenues coming from international businesses. Wockhardt is the only company in the world where USFDA has given QIDP Status (Qualified lnfectious Diseases Programme) for 5 of our Anti-bacterial discovery programmes - 2 of them are Gram Negative and 3 Gram Positive effective against untreatable Superbugs. Wockhardts entire Anti-infective portfolio particularly addresses the specific bacterial organism where resistances are high and breakthrough antibiotics are needed.Wockhardt Ltd was incorporated on July 8, 1999. In the year 2000, the company launched the cardiac drug enalapril maleate in the US through their marketing joint venture with Sidmak Laboratories. Also, they set up a corporate training centre with modern and state-of-the-art facility under one roof at Aurangabad. In the year 2001, the company terminated their three-year old marketing alliance with Sidmak Laboratories, one of the top ten generic Pharma companies in the US. Also, they entered into a strategic alliance with a Japanese firm Eisai Company Ltd to manufacture and market a neurology drug Methycobal. In the year 2003, the company restructured their field organization to upgrade their competitiveness and productivity, launched new four speciality hospitals at their Mulund complex in Mumbai. Also, they acquired CP pharmaceuticals (Holdings) Ltd, along with their subsidiaries. The company launched Asias first human recombinant insulin, making India the first Asian country to develop, manufacture and market the product. Also, they received USFDA approval for marketing bethanecol Chloride tablets in the US.In the year 2004, the company acquired the German pharmaceutical company esparma GmbH for a consideration of Rs 49 crore. Also, they got USFDA nod for 6 manufacturing units. In February 2005, the company launched Indias first automatic insulin delivery device specially designed for the convenience of Indian diabetic patients. The company forged alliance with Kamineni Group to establish two world-class heart hospitals in the Hyderabad. Also, they received US FDA approval for marketing cefuroxime axetil in the US market. In the year 2006, the US FDA had approved the companys Waluj plant.In the year 2007, the company signed in-licensing pact with Crawford Healthcare of UK. They acquired Negma Laboratories, which is the fourth largest independent, integrated pharmaceutical groups in France, for an all-cash deal worth $ 265 million. In October 2007, they acquired the Morton Grove Pharmaceuticals, a leading liquid generic and speciality dermatology company in the US. Also, they inked an in-licensing agreement with the Italy-based Gnosis, to market SAMe (S-adenosyl methionine). In the year 2008, the company approved demerger of their Research & Development business into a separate entity. Also, they launched the Cetirizine tablets in the USA. The company received the ANDA from the US FDA for marketing the tablets containing 5mg and 10mg Cetirizine Hydrochloride.In February 2008, they received approval from the US FDA for marketing the tablets containing 250 mg, 500 mg and 600 mg Azithromycin. In August 2008, the company received tentative approval from the US FDA to make and sell Sumatriptan Succinate injection, in the strength of 6-mg/0.5 ml. During the period January 2009 to March 2010, the company received 22 ANDA approval and launched eight new products, thereby expanding their product basket to 87. During the period, the company divested Animal Health Care Division to Vetoquinol, France. The business of Esparma GmbH was also divested to Mova GmbH.During the year 2010-11, the company launched a total of 43 new products in India. In April 2011, as per the scheme of arrangement, the Nutrition Business of Vinton Healthcare Ltd, a wholly owned subsidiary of the company was de-merged into the company. The appointed date for the Scheme is January 1, 2011.In January 2012, the company received final approval from the United States Food & Drug Administration (US FDA) for marketing 50 mcg nasal spray of Fluticasone which is used in treatment of allergic rhinitis.In 2012, the company launches generic version of anti--ulcer drug Prevacid. The company also receives US FDA approval for generic version of Parkinsonism drug Requip XL. The company receives tentative US FDA approval for generic version of anti-psychotic drug Geodon. The company also receives US FDA approval for generic version of Parkinsons drug Comtan.In 2013, the company Wockhardt receives the Best Enterprise award from the Europe. The company launches launches generic version of anti-convulsant drug Lamictal XR.In 2015, the company receives ANDA Approval for pain medication Oxycodone liquid. The company also receives Qualified Infectious Disease Product (QIDP) designation for its new Drug WCK 4873 from U.S. FDA. US FDA grants breakthrough (QIDP) drug discovery status to the New Antibiotic of Wockhardt.On 15 January 2016, Wockhardt Ltd informed the stock exchanges that inspection of its manufacturing unit at E-1/1, MIDC, Shendra, Aurangabad by US FDA has since been completed. US FDA has made 9 observations for which appropriate reply would be submitted to inspecting authority in due course. Shendra manufacturing unit is a new facility and presently there is no supply of products from the said Unit to USA markets.On 1 July 2016, Wockhardt Ltd informed the stock exchanges that the Company has given Corporate Guarantee to secure Term loan of US$ 250 Million facility availed by Wockhardt Bio AG, a subsidiary of the Company.On 8 August 2016, Wockhardt informed the stock exchanges that U.S. Food and Drug Administration (USFDA) has updated Import Alert 66-40 on its website on Wockhardts API (Active Pharmaceutical Ingredients) unit located in Ankleshwar, Gujarat. The company has already initiated required steps to address the concerns raised by USFDA and putting all efforts to resolve the matter. With reference to the earlier letter dated 8 August 2016 regarding Update on Import Alert 66-40 by US FDA on Wockhardts API Unit at Ankleshwar, Gujarat, Wockhardt Ltd informed the stock exchanges on 3 October 2016 that U.S. Food and Drug Administration (USFDA) on 30 September 2016 has posted on its website an update on the above referred matter and excluded the product Ceftriazone Sodium from Import Alert. This will enable the Company to manufacture and sell Ceftriazone API and formulation to US market.The Board of Directors of Wockhardt at their Meeting held on 10 November 2016 approved the acquisition of 100% stake in Wockhardt France (Holdings) S.A.S. (WFH) (an existing step down subsidiary of the Company) from Wockhardt Bio AG (WBG), a subsidiary of the Company. By virtue of the said acquisition, WFH shall become a direct wholly owned subsidiary of the Company from erstwhile step down subsidiary. WBG continues to be a direct subsidiary of the Company.On 23 November 2016, Wockhardt informed stock exchanges that U.S. Food and Drug Administration (USFDA) has issued a Warning Letter to C P Pharmaceuticals Limited, Wrexham, United Kingdom, a stepdown Subsidiary of the Company. Currently, there is no business being conducted from C P Pharmaceuticals to the US Market. C P Pharmaceuticals has already initiated required steps to address the concerns raised by USFDA and will be responding to the Agency within the prescribed time.On 13 December 2016, Wockhardt informed the stock exchanges that UK MHRA has since confirmed that the Companys manufacturing unit at Kadaiya, Daman complies with the principles and guidelines of Good Manufacturing Practices. In view of this, the approval status of the said unit continues.On 19 December 2016, Wockhardt informed the stock exchanges that UK MHRA has since confirmed that general compliance with the principles and guidelines of Good Manufacturing Practice of the Companys manufacturing unit at L-1, Chikalthana, Aurangabad. In view of this, the approval status of the said unit continues. Further, UK MHRA has considered the said manufacturing unit suitable for Risk based Inspection with reduced inspection frequency of 2 years from the existing inspection frequency of 1 year.On 5 January 2017, Wockhardt informed the stock exchanges that competent authority, Berlin, Germany has since issued EU GMP Certificate confirming that Companys manufacturing facility at 138, GIDC Estate, Ankaleshwar, Gujarat, complies with the principles and guidelines of Good Manufacturing Practices. The Certificate issued in this regard is valid for 3 years.On 1 March 2017, Wockhardt informed the stock exchanges that the U.S. Food and Drug Administration (USFDA) has issued a Warning Letter to Morton Grove Pharmaceuticals Inc., USA, a stepdown Subsidiary of the Company. This would mean that current portfolio of the Company will continue to be made available in the market. However, new approvals will be withheld till resolution. The Company, with the help of the Consultants, has already initiated appropriate measures since last several months to address the issues raised by USFDA.On 3 April 2017, Wockhardt announced that in a recent meeting between Wockhardt Research team and US FDA New Drug Antibiotic Regulatory team, US FDA agreed to abridged clinical trial for Phase III for Wockhardts superdrug antibiotic WCK 5222.This was based on the evaluation by US FDA of its preclinical and clinical data of Phase I establishing safety and clinical scope of efficacy for the drug. WCK 5222 is a combination of Zidebactam and Cefepime.On 29 May 2017, Wockhardt Limited (WL) announced that the Health Products Regulatory Authority of Ireland (HPRA) has granted Certificate of GMP Compliance to the companys Shendra, Aurangabad facility based on inspection performed from 27 February 2017 to 3 March 2017.On 22 June 2017, Wockhardt Limited (WL) announced that, WL and two subsidiaries, Wockhardt UK Holdings Limited and CP Pharmaceuticals Limited (CP), in the United Kingdom have settled an ongoing commercial litigation before the High Court in London, United Kingdom in related to a supply contract for a drug named Trisenox. The dispute between the parties was in respect of the price charged by CP to its counterparty to the contract, Cephalon Inc, (Cephalon) an affiliate of Teva Pharmaceuticals USA, Inc. (Teva). Under the above referred settlement between the parties, CP has agreed to waive its claim for the outstanding trade receivable of GBP 20 mn and accordingly dropped its counterclaim for the said amount and further paid a sum of GBP23 mn to Teva and Cephalon by way of full and final settlement of Tevas claims. The High Court has accepted the settlement between the parties and a Consent order was issued on 21 June 2017.On 7 August 2017, Wockhardt Limited announced that it has received approval from the United States Food & Drug Administration (US FDA) for an ANDA for 1gm, and 2gm injections of Oxacillin.Oxacillin is a penicillanase-resistant beta-lactam antibiotic and is used to treat many different infections caused by penicillin-resistant Staphylococcal and other bacterial infections, such as Urinary Tract Infections, Respiratory Tract Infections, Septicemia, Wound Infection, Bacterial meningitis etc. Wockhardt is expected to launch this product in the United States, soon. The product is being manufactured at a contract manufacturing facility, based near Milan, Italy.The Board of Directors of Wockhardt Limited at its meeting held on 4 May 2018 approved raising of additional capital by way of one or more public or private offerings including through a Qualified Institutions Placement (QIP) to eligible investors through an issuance of equity shares or other eligible securities for an amount not exceeding Rs 1500 crore as may be permitted under applicable law and subject to applicable regulatory and statutory approvals. With an aim to grow and further establish its international presence in pharmaceutical manufacturing, Wockhardt set up its first facility in Middle East for manufacturing of NCEs (New Chemical Entities) catering to the global markets through its Dubai arm of its subsidiary Wockhardt Bio AG in July 2018.On 12 October 2018, India Ratings and Research (Ind-Ra) downgraded Wockhardt Limiteds Long-Term Issuer Rating to IND BBB from IND A owing to on-going remediation costs being incurred, high R&D expenses, regulatory overhang etc.

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