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Metoprolol Tartrate

NDC 68645-191 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerLegacy Pharmaceutical Packaging, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA077739
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsMETOPROLOL TARTRATE (100 mg/1)
Marketing started20070911
Marketing ended20270731
Package count1

External sources

Source: openFDA. Public-domain (CC0).