FDA NDC Directory · JSON-LD · Markdown

Nadolol

NDC 68001-317 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerBluePoint Laboratories
Marketing categoryAbbreviated NDA (generic) · App ANDA203455
Dosage form / routeTABLET · ORAL
Active ingredientsNADOLOL (20 mg/1)
Marketing started20160223
Package count1

External sources

Source: openFDA. Public-domain (CC0).