FDA NDC Directory · JSON-LD · Markdown

Naproxen

NDC 52817-381 · HUMAN PRESCRIPTION DRUG · TABLET, DELAYED RELEASE

Labeler / ManufacturerTruPharma LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA216908
Dosage form / routeTABLET, DELAYED RELEASE · ORAL
Active ingredientsNAPROXEN (500 mg/1)
Marketing started20230727
Package count1

External sources

Source: openFDA. Public-domain (CC0).