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Metformin Hydrochloride

NDC 83301-0010 · HUMAN PRESCRIPTION DRUG · TABLET, COATED

Labeler / ManufacturerMullan Pharmaceutical Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA205096
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsMETFORMIN HYDROCHLORIDE (1000 mg/1)
Marketing started20240101
Package count3

External sources

Source: openFDA. Public-domain (CC0).