FDA NDC Directory · JSON-LD · Markdown

Nebivolol

NDC 67877-393 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAscend Laboratories, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA203828
Dosage form / routeTABLET · ORAL
Active ingredientsNEBIVOLOL HYDROCHLORIDE (2.5 mg/1)
Marketing started20210916
Package count4

External sources

Source: openFDA. Public-domain (CC0).