Lupin Limited has informed the Exchange regarding a press release dated October 08, 2026, titled "Lupin Receives U.S. FDA Approval for Phytonadione Injectable Emulsion, USP".
Filed with NSE · ISIN INE326A01029 · · 2 pages · English
Summary by 6ix AI
The approval is for a single-dose prefilled syringe formulation, which is indicated for treating low blood clotting and vitamin K deficiency. This filing serves to inform the exchange and the public about the regulatory approval and its significance for Lupin's product portfolio.
Written by 6ix AI from the company’s filing. How 6ix writes summaries
We are pleased to enclose a Press Release titled “Lupin Receives U.S. FDA Approval for Phytonadione Injectable Emulsion, USP”. The same is for your information and dissemination. AMIT KUMAR GUPTA COMPANY SECRETARY & COMPLIANCE OFFICER (ACS -15754) Encl.: a/a. Corporate Identity Number: L24100MH1983PLC029442 info@lupin.com | www.lupin.com Press Release BSE: 500257 NSE: LUPIN REUTERS: LUPIN.BO BLOOM
Story so far
- Lupin Limited has informed the Exchange regarding a press release dated October 06, 2026, titled "Lupin Launches Formoflo-G® MDI, World s First Fixed-dose Triple Combination Drug for COPD Management".
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Earlier from Lupin
- Lupin Limited has informed the Exchange regarding a press release dated October 06, 2026, titled "Lupin Launches Formoflo-G® MDI, World s First Fixed-dose Triple Combination Drug for COPD Management".
- Lupin Receives Tentative Approval from U.S. FDA for Novel Apixaban Oral Suspension
- Lupin Limited Press Release Sep 28 2026
- Lupin Receives U.S. FDA Approval for Modafinil Tablets, USP
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