FDA NDC Directory · JSON-LD · Markdown

Naproxen Sodium

NDC 41250-477 · HUMAN OTC DRUG · TABLET, FILM COATED

Labeler / ManufacturerMeijer Distribution Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA074661
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsNAPROXEN SODIUM (220 mg/1)
Marketing started20140305
Package count4

External sources

Source: openFDA. Public-domain (CC0).