FDA NDC Directory · JSON-LD · Markdown

Naproxen sodium

NDC 55700-625 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerQuality Care Products, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA078486
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsNAPROXEN SODIUM (550 mg/1)
Marketing started20180518
Marketing ended20261031
Package count1

External sources

Source: openFDA. Public-domain (CC0).