FDA NDC Directory · JSON-LD · Markdown

NEBIVOLOL

NDC 70518-4032 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namenebivolol
Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA212682
Dosage form / routeTABLET · ORAL
Active ingredientsNEBIVOLOL (5 mg/1)
Marketing started20240305
Package count1

External sources

Source: openFDA. Public-domain (CC0).