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metoprolol succinate

NDC 70771-1341 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerZydus Lifesciences Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA203894
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsMETOPROLOL SUCCINATE (200 mg/1)
Marketing started20180607
Package count3

External sources

Source: openFDA. Public-domain (CC0).