FDA NDC Directory · JSON-LD · Markdown

Medique Mediproxen

NDC 85766-121 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic nameNAPROXEN SODIUM
Labeler / ManufacturerSportpharm LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA079096
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsNAPROXEN SODIUM (220 mg/1)
Marketing started20081230
Package count3

External sources

Source: openFDA. Public-domain (CC0).