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METFORMIN HYDROCHLORIDE

NDC 71610-837 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Generic namemetformin hydrochloride
Labeler / ManufacturerAphena Pharma Solutions - Tennessee, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA201991
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsMETFORMIN HYDROCHLORIDE (500 mg/1)
Marketing started20130301
Package count6

External sources

Source: openFDA. Public-domain (CC0).