FDA NDC Directory · JSON-LD · Markdown

Nebivolol

NDC 70756-293 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerLifestar Pharma LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA216172
Dosage form / routeTABLET · ORAL
Active ingredientsNEBIVOLOL HYDROCHLORIDE (20 mg/1)
Marketing started20221114
Package count2

External sources

Source: openFDA. Public-domain (CC0).