FDA NDC Directory · JSON-LD · Markdown

naproxen sodium pm

NDC 30142-753 · HUMAN OTC DRUG · TABLET

Generic namediphenhydramine hydrochloride, naproxen sodium
Labeler / ManufacturerKroger Company
Marketing categoryAbbreviated NDA (generic) · App ANDA208499
Dosage form / routeTABLET · ORAL
Active ingredientsDIPHENHYDRAMINE HYDROCHLORIDE (25 mg/1)
NAPROXEN SODIUM (220 mg/1)
Marketing started20190620
Package count1

External sources

Source: openFDA. Public-domain (CC0).