Lupin gets tentative USFDA nod for Sitagliptin, Metformin Hydrochloride Tablets to treat type 2 diabetes
Mumbai: Global pharma major Lupin Limited today announced that it has received tentative approval from the United States Food and Drug Administration (USFDA) for its Abbreviated New Drug Application for Sitagliptin and Metformin Hydrochloride Tablets, 50 mg/500 mg and 50 mg/1000 mg, to market a generic equivalent of Janumet Tablets, 50 mg/500 mg and 50 mg/1000 mg of Merck Sharp & Dohme LLC. This product will be manufactured at Lupin’s Pithampur facility in India.
Sitagliptin and Metformin Hydrochloride Tablets, 50 mg/500 mg and 50 mg/1000 mg are indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus.
Sitagliptin and Metformin Hydrochloride Tablets, 50 mg/500 mg and 50 mg/1000 mg (RLD Janumet Tablets) had an estimated annual sale of USD 1,145 million in the U.S. (IQVIA MAT September 2024).
Read also: Lupin's generic drug to treat ADHD symptoms gets USFDA approval
Lupin Limited is a global pharmaceutical leader headquartered in Mumbai, India, with products distributed in over 100 markets. Lupin specializes in pharmaceutical products, including branded and generic formulations, complex generics, biotechnology products, and active pharmaceutical ingredients. The company has a strong position in India and the U.S. across multiple therapy areas, including respiratory, cardiovascular, anti-diabetic, anti-infective, gastrointestinal, central nervous system, and women’s health. Lupin has 15 state-of-the-art manufacturing sites and 7 research centers globally.
