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up and up naproxen sodium pm

NDC 11673-687 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic namediphenhydramine hydrochloride, naproxen sodium
Labeler / ManufacturerTarget Corporation
Marketing categoryAbbreviated NDA (generic) · App ANDA208499
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsDIPHENHYDRAMINE HYDROCHLORIDE (25 mg/1)
NAPROXEN SODIUM (220 mg/1)
Marketing started20220125
Package count1

External sources

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