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Saxagliptin and Metformin Hydrochloride

NDC 43598-620 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerDr.Reddys Laboratories Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA207678
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsMETFORMIN HYDROCHLORIDE (500 mg/1)
SAXAGLIPTIN (5 mg/1)
Marketing started20230809
Package count1

External sources

Source: openFDA. Public-domain (CC0).