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Glenmark Pharmaceuticals informs about press release

01 Dec 2025 Evaluate

Pursuant to Regulation 30 of the SEBI (Listing Obligations & Disclosure Requirements) Regulations, 2015, Glenmark Pharmaceuticals has informed that the U.S. Food and Drug Administration (U.S. FDA) completed Pre-Approval Inspection at the Company’s formulations manufacturing facility in Chhatrapati Sambhajinagar (Aurangabad). The inspection was carried out from November 24 to November 28, 2025, and concluded with zero 483 observations.

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

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