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Saxagliptin

NDC 0378-4706 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namesaxagliptin
Labeler / ManufacturerMylan Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA205980
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsSAXAGLIPTIN HYDROCHLORIDE DIHYDRATE (5 mg/1)
Marketing started20230804
Package count2

External sources

Source: openFDA. Public-domain (CC0).