FDA NDC Directory · JSON-LD · Markdown

All Day Pain Relief

NDC 79903-005 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic nameNaproxen Sodium
Labeler / ManufacturerWALMART INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA204872
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsNAPROXEN SODIUM (220 mg/1)
Marketing started20201022
Package count4

External sources

Source: openFDA. Public-domain (CC0).