FDA NDC Directory · JSON-LD · Markdown

Nadolol

NDC 69238-1123 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAmneal Pharmaceuticals NY LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA208832
Dosage form / routeTABLET · ORAL
Active ingredientsNADOLOL (20 mg/1)
Marketing started20170602
Package count3

External sources

Source: openFDA. Public-domain (CC0).