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METOPROLOL TARTRATE

NDC 69367-355 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namemetoprolol tartrate
Labeler / ManufacturerWestminster Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA074453
Dosage form / routeTABLET · ORAL
Active ingredientsMETOPROLOL TARTRATE (100 mg/1)
Marketing started20231218
Marketing ended20260731
Package count2

External sources

Source: openFDA. Public-domain (CC0).