FDA NDC Directory · JSON-LD · Markdown

Nadolol

NDC 69097-869 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerCipla USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA203455
Dosage form / routeTABLET · ORAL
Active ingredientsNADOLOL (80 mg/1)
Marketing started20160223
Package count3

External sources

Source: openFDA. Public-domain (CC0).