FDA NDC Directory · JSON-LD · Markdown

foster and thrive all day pain relief

NDC 70677-1137 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic nameNaproxen Sodium
Labeler / ManufacturerStrategic Sourcing Services LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA074661
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsNAPROXEN SODIUM (220 mg/1)
Marketing started20230914
Package count2

External sources

Source: openFDA. Public-domain (CC0).