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Bisoprolol

NDC 42571-470 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameBisoprolol Fumarate
Labeler / ManufacturerMicro Labs Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA218303
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsBISOPROLOL FUMARATE (5 mg/1)
Marketing started20260601
Package count3

External sources

Source: openFDA. Public-domain (CC0).