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Metoprolol Tartrate

NDC 48433-074 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namemetoprolol tartrate
Labeler / ManufacturerSafecor Health, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA076704
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsMETOPROLOL TARTRATE (50 mg/1)
Marketing started20260216
Package count1

External sources

Source: openFDA. Public-domain (CC0).