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Bisoprolol Fumarate

NDC 52817-268 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerTruPharma LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA075643
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsBISOPROLOL FUMARATE (2.5 mg/1)
Marketing started20250307
Package count1

External sources

Source: openFDA. Public-domain (CC0).