FDA NDC Directory · JSON-LD · Markdown

Naproxen Sodium

NDC 21130-856 · HUMAN OTC DRUG · TABLET, FILM COATED

Labeler / ManufacturerBetter Living Brands, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA204872
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsNAPROXEN SODIUM (220 mg/1)
Marketing started20231011
Package count1

External sources

Source: openFDA. Public-domain (CC0).