Zydus Lifesciences Limited announced that the US Food and Drug Administration (FDA) has 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.
The approval of Zituvimet is based on research, development, regulatory, and manufacturing work performed by Zydus teams. Zituvimet has undergone quality testing for nitrosamines and potential genotoxic impurities as per current US FDA standards. Zituvimet is compliant with current US FDA standards of Nitrosamines in sitagliptin containing products.
“The Zituvimet approval further builds on our previous approval of Zituvio (sitagliptin) and offers an increased accessibility and affordability to healthcare systems with regard to prescription drugs for type II diabetes. The Zituvimet approval provides an affordable treatment option for healthcare systems to reduce the rate of growth in drug spending and improves the financial sustainability of the healthcare programmes,” said Dr Sharvil Patel, managing director of Zydus Lifesciences Limited.
The Zydus Group with an overarching purpose of empowering people with freedom to live healthier and more fulfilled lives, is an innovative, global life sciences company that discovers, develops, manufactures, and markets a broad range of healthcare therapies.
