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Metformin Hydrochloride

NDC 71709-111 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerMetcure Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA090564
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsMETFORMIN HYDROCHLORIDE (850 mg/1)
Marketing started20171114
Package count2

External sources

Source: openFDA. Public-domain (CC0).