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METFORMIN HYDROCHLORIDE

NDC 50228-588 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerScieGen Pharmaceuticals Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA203769
Dosage form / routeTABLET · ORAL
Active ingredientsMETFORMIN HYDROCHLORIDE (625 mg/1)
Marketing started20260821
Package count2

External sources

Source: openFDA. Public-domain (CC0).