FDA NDC Directory · JSON-LD · Markdown

Nebivolol Hydrochloride

NDC 29300-377 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerUnichem Pharmaceuticals (USA), Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA213830
Dosage form / routeTABLET · ORAL
Active ingredientsNEBIVOLOL HYDROCHLORIDE (10 mg/1)
Marketing started20220404
Package count3

External sources

Source: openFDA. Public-domain (CC0).