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METFORMIN HYDROCHLORIDE

NDC 69367-413 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerWestminster Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA203832
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsMETFORMIN HYDROCHLORIDE (1000 mg/1)
Marketing started20251023
Package count1

External sources

Source: openFDA. Public-domain (CC0).