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METFORMIN HYDROCHLORIDE

NDC 68788-8564 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namemetformin hydrochloride
Labeler / ManufacturerPreferred Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA213320
Dosage form / routeTABLET · ORAL
Active ingredientsMETFORMIN HYDROCHLORIDE (500 mg/1)
Marketing started20240111
Marketing ended20260930
Package count1

External sources

Source: openFDA. Public-domain (CC0).