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Metoprolol Tartrate

NDC 55289-382 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namemetoprolol tartrate
Labeler / ManufacturerPD-Rx Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA076704
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsMETOPROLOL TARTRATE (25 mg/1)
Marketing started20040223
Package count5

External sources

Source: openFDA. Public-domain (CC0).