FDA NDC Directory · JSON-LD · Markdown

Naproxen

NDC 68788-7572 · HUMAN OTC DRUG · TABLET

Generic nameNaproxen Sodium
Labeler / ManufacturerPreferred Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA204872
Dosage form / routeTABLET · ORAL
Active ingredientsNAPROXEN SODIUM (220 mg/1)
Marketing started20190101
Package count4

External sources

Source: openFDA. Public-domain (CC0).