FDA NDC Directory · JSON-LD · Markdown

naproxen sodium

NDC 72288-988 · HUMAN OTC DRUG · TABLET, FILM COATED

Labeler / ManufacturerAmazon.com Services LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA074661
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsNAPROXEN SODIUM (220 mg/1)
Marketing started20260903
Package count1

External sources

Source: openFDA. Public-domain (CC0).