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nebivolol

NDC 68462-618 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namenebivolol hydrochloride
Labeler / ManufacturerGlenmark Pharmaceuticals Inc., USA
Marketing categoryAbbreviated NDA (generic) · App ANDA203821
Dosage form / routeTABLET · ORAL
Active ingredientsNEBIVOLOL HYDROCHLORIDE (20 mg/1)
Marketing started20170525
Package count3

External sources

Source: openFDA. Public-domain (CC0).