Zydus Lifesciences wins USFDA nod for diabetes drug Zituvimet
The approval of ZITUVIMET is based on research, development, regulatory, and manufacturing work performed by Zydus teams.;
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Ahmedabad: Pharma major, Zydus Lifesciences Limited, today announced that the U.S. Food and Drug Administration (USFDA) approved its New Drug Application (NDA) for ZITUVIMET (Sitagliptin and Metformin hydrochloride) tablets, 50 mg/500 mg and 50 mg/1000 mg.
ZITUVIMET contains active ingredients sitagliptin, a dipeptidyl peptidase-4 (DPP-4) inhibitor, and metformin hydrochloride (HCl), a biguanide, indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus.
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