Lupin informs about press release

17 Nov 2023 Evaluate

Lupin has informed that it enclosed a Press release regarding receipt of US FDA approval for the Company’s Abbreviated New Drug Application for Ganirelix Acetate Injection, 250 mcg/0.5 mL Single-Dose Prefilled Syringe, to market a generic equivalent to the reference listed drug of Ganirelix Acetate Injection, 250 mcg/0.5 mL of Organon USA LLC. 

The above information is a part of company’s filings submitted to BSE.

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