FDA NDC Directory · JSON-LD · Markdown

Naproxen Sodium

NDC 55111-272 · HUMAN OTC DRUG · TABLET, COATED

Labeler / ManufacturerDr.Reddy's Laboratories Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA075168
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsNAPROXEN SODIUM (220 mg/1)
Marketing started19980729
Package count5

External sources

Source: openFDA. Public-domain (CC0).