FDA NDC Directory · JSON-LD · Markdown

All Day Pain Relief

NDC 59428-604 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic nameNaproxen Sodium
Labeler / ManufacturerZapotol Products Corp
Marketing categoryAbbreviated NDA (generic) · App ANDA204872
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsNAPROXEN SODIUM (220 mg/1)
Marketing started20201022
Package count1

External sources

Source: openFDA. Public-domain (CC0).