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Naproxen Sodium and Diphenhydramine HCl

NDC 62207-814 · HUMAN OTC DRUG · TABLET, FILM COATED

Labeler / ManufacturerGranules India Ltd
Marketing categoryAbbreviated NDA (generic) · App ANDA213663
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsDIPHENHYDRAMINE HYDROCHLORIDE (25 mg/1)
NAPROXEN SODIUM (220 mg/1)
Marketing started20210220
Package count4

External sources

Source: openFDA. Public-domain (CC0).