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Naproxen Sodium

NDC 58602-845 · HUMAN OTC DRUG · TABLET, FILM COATED

Labeler / ManufacturerAurohealth LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA205497
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsNAPROXEN SODIUM (220 mg/1)
Marketing started20200516
Package count1

External sources

Source: openFDA. Public-domain (CC0).