FDA NDC Directory · JSON-LD · Markdown

NAPROXEN

NDC 43063-920 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerPD-Rx Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA091416
Dosage form / routeTABLET · ORAL
Active ingredientsNAPROXEN (500 mg/1)
Marketing started20160706
Package count9

External sources

Source: openFDA. Public-domain (CC0).