FDA NDC Directory · JSON-LD · Markdown

All Day Pain Relief

NDC 69517-109 · HUMAN OTC DRUG · TABLET

Generic nameNaproxen Sodium Tablets, 220 mg
Labeler / ManufacturerHealthLife of USA LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA091353
Dosage form / routeTABLET · ORAL
Active ingredientsNAPROXEN SODIUM (220 mg/1)
Marketing started20110930
Package count4

External sources

Source: openFDA. Public-domain (CC0).