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Metformin hydrochloride

NDC 68071-1419 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerNuCare Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA201991
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsMETFORMIN HYDROCHLORIDE (500 mg/1)
Marketing started20130301
Package count5

External sources

Source: openFDA. Public-domain (CC0).