FDA NDC Directory · JSON-LD · Markdown

NAPROXEN SODIUM

NDC 57344-145 · HUMAN OTC DRUG · TABLET, COATED

Labeler / ManufacturerAAA Pharmaceutical, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA079096
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsNAPROXEN SODIUM (220 mg/1)
Marketing started20120401
Package count1

External sources

Source: openFDA. Public-domain (CC0).