FDA NDC Directory · JSON-LD · Markdown

Nebivolol

NDC 70518-3527 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA203828
Dosage form / routeTABLET · ORAL
Active ingredientsNEBIVOLOL HYDROCHLORIDE (5 mg/1)
Marketing started20220920
Package count1

External sources

Source: openFDA. Public-domain (CC0).