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Metoprolol Succinate

NDC 68001-501 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Generic nameMetoprolol Succinate ER Tablets
Labeler / ManufacturerBluePoint Laboratories
Marketing categoryAbbreviated NDA (generic) · App ANDA211143
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsMETOPROLOL SUCCINATE (50 mg/1)
Marketing started20210514
Package count2

External sources

Source: openFDA. Public-domain (CC0).