FDA NDC Directory · JSON-LD · Markdown

Naproxen

NDC 21130-062 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerSafeway, Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA091353
Dosage form / routeTABLET · ORAL
Active ingredientsNAPROXEN SODIUM (220 mg/1)
Marketing started20230830
Package count3

External sources

Source: openFDA. Public-domain (CC0).