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METOPROLOL SUCCINATE

NDC 31722-591 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerCamber Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA205541
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsMETOPROLOL SUCCINATE (100 mg/1)
Marketing started20201106
Package count4

External sources

Source: openFDA. Public-domain (CC0).