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naproxen sodium pm

NDC 41250-526 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic namediphenhydramine hydrochloride, naproxen sodium
Labeler / ManufacturerMeijer Distribution Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA208499
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsDIPHENHYDRAMINE HYDROCHLORIDE (25 mg/1)
NAPROXEN SODIUM (220 mg/1)
Marketing started20200114
Package count2

External sources

Source: openFDA. Public-domain (CC0).