FDA NDC Directory · JSON-LD · Markdown

Naproxen Sodium

NDC 63868-465 · HUMAN OTC DRUG · TABLET, COATED

Generic nameNAPROXEN SODIUM
Labeler / ManufacturerChain Drug Marketing Association
Marketing categoryAbbreviated NDA (generic) · App ANDA079096
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsNAPROXEN SODIUM (220 mg/1)
Marketing started20090903
Marketing ended20271231
Package count2

External sources

Source: openFDA. Public-domain (CC0).