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Naproxen Sodium Diphenhydramine Hydrochloride

NDC 21130-814 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerSAFEWAY
Marketing categoryAbbreviated NDA (generic) · App ANDA213663
Dosage form / routeTABLET · ORAL
Active ingredientsDIPHENHYDRAMINE HYDROCHLORIDE (25 mg/1)
NAPROXEN SODIUM (220 mg/1)
Marketing started20230630
Package count1

External sources

Source: openFDA. Public-domain (CC0).