FDA NDC Directory · JSON-LD · Markdown

All Day Pain Relief

NDC 79903-389 · HUMAN OTC DRUG · TABLET

Generic nameNaproxen Sodium
Labeler / ManufacturerWalmart Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA090545
Dosage form / routeTABLET · ORAL
Active ingredientsNAPROXEN SODIUM (220 mg/1)
Marketing started20250510
Package count1

External sources

Source: openFDA. Public-domain (CC0).