FDA NDC Directory · JSON-LD · Markdown

Nebivolol

NDC 72241-034 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerModavar Pharmaceuticals LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA208717
Dosage form / routeTABLET · ORAL
Active ingredientsNEBIVOLOL HYDROCHLORIDE (10 mg/1)
Marketing started20171229
Package count4

External sources

Source: openFDA. Public-domain (CC0).