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Metformin Hydrochloride

NDC 68788-8520 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerPreferred Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA090692
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsMETFORMIN HYDROCHLORIDE (1000 mg/1)
Marketing started20230901
Package count1

External sources

Source: openFDA. Public-domain (CC0).