FDA NDC Directory · JSON-LD · Markdown

Nadolol

NDC 70518-4662 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA201893
Dosage form / routeTABLET · ORAL
Active ingredientsNADOLOL (40 mg/1)
Marketing started20260518
Package count1

External sources

Source: openFDA. Public-domain (CC0).