FDA NDC Directory · JSON-LD · Markdown

CareOne Naproxen Sodium

NDC 41520-507 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic nameNaproxen Sodium
Labeler / ManufacturerAmerican Sales Company
Marketing categoryAbbreviated NDA (generic) · App ANDA074661
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsNAPROXEN SODIUM (220 mg/1)
Marketing started20160805
Package count3

External sources

Source: openFDA. Public-domain (CC0).