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Metformin Hydrochloride

NDC 0378-6002 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Generic namemetformin
Labeler / ManufacturerMylan Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA200690
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsMETFORMIN HYDROCHLORIDE (500 mg/1)
Marketing started20160823
Package count1

External sources

Source: openFDA. Public-domain (CC0).