FDA NDC Directory · JSON-LD · Markdown

All Day Relief

NDC 56062-368 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic nameNaproxen Sodium
Labeler / ManufacturerPublix Super Markets Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA074661
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsNAPROXEN SODIUM (220 mg/1)
Marketing started19971229
Package count3

External sources

Source: openFDA. Public-domain (CC0).