FDA NDC Directory · JSON-LD · Markdown

NADOLOL

NDC 62332-402 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAlembic Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA211763
Dosage form / routeTABLET · ORAL
Active ingredientsNADOLOL (20 mg/1)
Marketing started20230608
Package count3

External sources

Source: openFDA. Public-domain (CC0).