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.