FDA NDC Directory · JSON-LD · Markdown

Leader All Day Pain Relief

NDC 70000-0201 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic nameNaproxen Sodium
Labeler / ManufacturerCardinal Health 110, LLC. dba Leader
Marketing categoryAbbreviated NDA (generic) · App ANDA074661
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsNAPROXEN SODIUM (220 mg/1)
Marketing started20161207
Package count3

External sources

Source: openFDA. Public-domain (CC0).