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Naproxen Sodium and Diphenhydramine HCL

NDC 11673-819 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerTARGET CORPORATION
Marketing categoryAbbreviated NDA (generic) · App ANDA213663
Dosage form / routeTABLET · ORAL
Active ingredientsDIPHENHYDRAMINE HYDROCHLORIDE (25 mg/1)
NAPROXEN SODIUM (220 mg/1)
Marketing started20240301
Package count1

External sources

Source: openFDA. Public-domain (CC0).