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up and up naproxen sodium

NDC 11673-909 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic namenaproxen sodium
Labeler / ManufacturerTarget Corporation
Marketing categoryAbbreviated NDA (generic) · App ANDA074661
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsNAPROXEN SODIUM (220 mg/1)
Marketing started20200214
Package count1

External sources

Source: openFDA. Public-domain (CC0).