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Metoprolol Tartrate

NDC 52817-359 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerTruPharma LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA200981
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsMETOPROLOL TARTRATE (75 mg/1)
Marketing started20181201
Package count2

External sources

Source: openFDA. Public-domain (CC0).