FDA NDC Directory · JSON-LD · Markdown

naproxen sodium pm

NDC 37808-264 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic namediphenhydramine hydrochloride, naproxen sodium
Labeler / ManufacturerH E B
Marketing categoryAbbreviated NDA (generic) · App ANDA208499
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsDIPHENHYDRAMINE HYDROCHLORIDE (25 mg/1)
NAPROXEN SODIUM (220 mg/1)
Marketing started20201013
Package count2

External sources

Source: openFDA. Public-domain (CC0).