FDA NDC Directory · JSON-LD · Markdown

NAPROXEN SODIUM

NDC 51013-137 · HUMAN OTC DRUG · CAPSULE, LIQUID FILLED

Generic nameNaproxen Sodium
Labeler / ManufacturerPuraCap Pharmaceutical LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA208363
Dosage form / routeCAPSULE, LIQUID FILLED · ORAL
Active ingredientsNAPROXEN SODIUM (220 mg/1)
Marketing started20180320
Package count3

External sources

Source: openFDA. Public-domain (CC0).