FDA NDC Directory · JSON-LD · Markdown

AnaDent

NDC 27854-170 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic nameNaproxen Sodium
Labeler / ManufacturerBelmora LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA204872
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsNAPROXEN SODIUM (220 mg/1)
Marketing started20170123
Package count1

External sources

Source: openFDA. Public-domain (CC0).