FDA NDC Directory · JSON-LD · Markdown

All Day Pain Relief

NDC 59726-169 · HUMAN OTC DRUG · TABLET

Generic nameNaproxen sodium
Labeler / ManufacturerP & L Development, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA079096
Dosage form / routeTABLET · ORAL
Active ingredientsNAPROXEN SODIUM (220 mg/1)
Marketing started20140228
Package count2

External sources

Source: openFDA. Public-domain (CC0).