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Bisoprolol Fumarate

NDC 16714-529 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerNorthStar Rx LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA077910
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsBISOPROLOL FUMARATE (5 mg/1)
Marketing started20061227
Package count2

External sources

Source: openFDA. Public-domain (CC0).