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Glipizide and Metformin Hydrochloride

NDC 68382-184 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerZydus Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA078905
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsGLIPIZIDE (2.5 mg/1)
METFORMIN HYDROCHLORIDE (250 mg/1)
Marketing started20160505
Package count4

External sources

Source: openFDA. Public-domain (CC0).