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Metoprolol Succinate

NDC 70010-783 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerGranules Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA216916
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsMETOPROLOL SUCCINATE (200 mg/1)
Marketing started20231002
Package count3

External sources

Source: openFDA. Public-domain (CC0).