FDA NDC Directory · JSON-LD · Markdown

Naproxen Sodium

NDC 50844-604 · HUMAN OTC DRUG · TABLET, FILM COATED

Labeler / ManufacturerL.N.K. International, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA204872
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsNAPROXEN SODIUM (220 mg/1)
Marketing started20170201
Package count9

External sources

Source: openFDA. Public-domain (CC0).