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Metoprolol succinate

NDC 72789-284 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerPD-Rx Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA090617
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsMETOPROLOL SUCCINATE (50 mg/1)
Marketing started20120910
Package count2

External sources

Source: openFDA. Public-domain (CC0).