Categories: US FDA Approval

Zydus Cadila gets USFDA’s nod for Sitagliptin and Met form in Hydro chloride Tablets

Mumbai, July 26, 2017: Zydus Cadila has received the tentative approval from the US Food and Drug Administration (USFDA) to market Sitagliptin and Met for min Hydro chloride Tablets in the strengths of 50 mg/500 mg and 50 mg/1000 mg. This is a fixed dose combination of two anti-diabetic drugs indicated for Type H diabetes mellitus and will be produced at the group’s formulations manufacturing facility at the Pharma SEZ in Ahmedabad. The group now has more than 120 approvals and has so far filed over 300 ANDAs since the commencement of the filing process in FY 2003-04. Zydus Cadila is an innovative, global pharmaceutical company that discovers, develops, manufactures and markets a broad range of healthcare therapies.

United News Of India

The Pharma Times News Bureau

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