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Naproxen

NDC 50844-261 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic nameNaproxen Sodium
Labeler / ManufacturerL.N.K. International, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA204872
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsNAPROXEN SODIUM (220 mg/1)
Marketing started20190806
Package count1

External sources

Source: openFDA. Public-domain (CC0).