Glenmark Pharmaceuticals informs about press release

04 Mar 2026 Evaluate
Glenmark Pharmaceuticals has informed that, Glenmark Specialty SA (Glenmark) has received final approval by the United States Food & Drug Administration (U.S. FDA) for Fluticasone Propionate Inhalation Aerosol USP, 44 mcg per actuation. The press release in this regard is attached.

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

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