FDA NDC Directory · JSON-LD · Markdown

Naproxen Sodium

NDC 37835-594 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerBi-Mart
Marketing categoryAbbreviated NDA (generic) · App ANDA091353
Dosage form / routeTABLET · ORAL
Active ingredientsNAPROXEN SODIUM (220 mg/1)
Marketing started20110930
Package count2

External sources

Source: openFDA. Public-domain (CC0).