FDA NDC Directory · JSON-LD · Markdown

Naproxen Sodium

NDC 69848-010 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerGranules USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA091353
Dosage form / routeTABLET · ORAL
Active ingredientsNAPROXEN SODIUM (220 mg/1)
Marketing started20190701
Package count3

External sources

Source: openFDA. Public-domain (CC0).