FDA NDC Directory · JSON-LD · Markdown

Naproxen sodium

NDC 69230-329 · HUMAN OTC DRUG · TABLET, FILM COATED

Labeler / ManufacturerCamber Consumer Care Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA211065
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsNAPROXEN SODIUM (220 mg/1)
Marketing started20221028
Package count6

External sources

Source: openFDA. Public-domain (CC0).