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Metformin Hydrochloride

NDC 71610-929 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAphena Pharma Solutions - Tennessee, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA077095
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsMETFORMIN HYDROCHLORIDE (500 mg/1)
Marketing started20240329
Package count6

External sources

Source: openFDA. Public-domain (CC0).