FDA NDC Directory · JSON-LD · Markdown

Nebivolol

NDC 31722-587 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerCamber Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA203825
Dosage form / routeTABLET · ORAL
Active ingredientsNEBIVOLOL HYDROCHLORIDE (10 mg/1)
Marketing started20210917
Package count5

External sources

Source: openFDA. Public-domain (CC0).