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Metoprolol Succinate

NDC 68001-360 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerBluePoint Laboratories
Marketing categoryAbbreviated NDA (generic) · App ANDA204106
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsMETOPROLOL SUCCINATE (200 mg/1)
Marketing started20180629
Package count2

External sources

Source: openFDA. Public-domain (CC0).