NSEGeneral Updates2d ago · 28 Aug 2026, 09:11 pm
General Updates
Cipla Limited · CIPLA
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Cipla Limited has informed the Exchange about the outcome of the USFDA inspection at its InvaGen manufacturing facility in Central Islip, Long Island, NY, USA, which has been classified as Voluntary Action Indicated (VAI).
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Cipla Limited has informed the Exchange about Update on USFDA inspection at InvaGen manufacturing facility in Central Islip, Long Island, NY, USA
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28th August, 2026
(1) BSE Limited (2) National Stock Exchange of India Limited
Listing Department, Listing Department
Phiroze Jeejeebhoy Towers, Exchange Plaza, 5th floor,
Dalal Street, Plot no. C/1, G Block,
Mumbai 400 001 Bandra Kurla Complex,
Bandra (East), Mumbai - 400 051
Scrip Code: 500087 Scrip Code: CIPLA
(3) SOCIETE DE LA BOURSE DE LUXEMBOURG
Societe Anonyme
35A Boulevard Joseph II,
L-1840 Luxembourg
Dear Sir/Madam,
Sub: Update on USFDA inspection at InvaGen manufacturing facility in Central Islip, Long Island, NY,
Dear Sir/Madam,
Pursuant to Regulation 30 of the SEBI (Listing Obligations and Disclosure Requirements) Regulations,
2015, and further to our intimation dated 18th July, 2026 regarding the United States Food and Drug
Administration (USFDA) inspection conducted at the Unit 3 manufacturing facility of InvaGen
Pharmaceuticals Inc. (wholly owned subsidiary of the Company) located in Central Islip, Long Island, New
York, USA, from 13th July, 2026 to 17th July, 2026 (EDT), we hereby notify that the USFDA vide
communication dated 28th August, 2026 has classified the above referred inspection as Voluntary Action
Indicated (VAI).
Kindly take the above information on record.
Yours faithfully,
For Cipla Limited
Rajendra Chopra
Company Secretary
Prepared by: Simona Dsouza
Cipla Ltd.
Regd. Office - Cipla House, Peninsula Business Park, Ganpatrao Kadam Marg, Lower Parel, Mumbai-400 013, India
P +91 22 24826000 W www.cipla.com E-mail contactus@cipla.com Corporate Identity Number L24239MH1935PLC002380