Mumbai, July 14 -- The USFDA inspection was conducted between 3 February and 14 February 2025.

In an official filing, the company stated that it does not anticipate the warning letter will disrupt supply chains or affect revenues generated from the Indore facility. Glenmark emphasized its commitment to addressing the FDA's concerns promptly and working closely with the regulator to resolve the issues.

The company further clarified that there were no observations related to data integrity during the inspection. Glenmark reaffirmed its dedication to maintaining the highest quality and compliance standards, including adherence to Current Good Manufacturing Practices (CGMP), across all its facilities.

Glenmark Pharmaceuticals is a research...