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Glumetza

NDC 68012-002 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Generic namemetformin hydrochloride
Labeler / ManufacturerSantarus, Inc.
Marketing categoryNew Drug Application (innovator) · App NDA021748
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsMETFORMIN HYDROCHLORIDE (500 mg/1)
Marketing started20060801
Package count1

External sources

Source: openFDA. Public-domain (CC0).