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Metoprolol Tartrate

NDC 59651-758 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA077739
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsMETOPROLOL TARTRATE (37.5 mg/1)
Marketing started20231207
Package count1

External sources

Source: openFDA. Public-domain (CC0).