FDA NDC Directory · JSON-LD · Markdown

NEBIVOLOL

NDC 0904-7498 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namenebivolol
Labeler / ManufacturerMajor Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA212682
Dosage form / routeTABLET · ORAL
Active ingredientsNEBIVOLOL (5 mg/1)
Marketing started20250224
Package count1

External sources

Source: openFDA. Public-domain (CC0).