FDA NDC Directory · JSON-LD · Markdown

Naproxen

NDC 72789-321 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerPD-Rx Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA212517
Dosage form / routeTABLET · ORAL
Active ingredientsNAPROXEN (500 mg/1)
Marketing started20200301
Package count6

External sources

Source: openFDA. Public-domain (CC0).