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Naproxen Sodium PM

NDC 62011-0396 · HUMAN OTC DRUG · TABLET

Generic nameNaproxen Sodium
Labeler / ManufacturerStrategic Sourcing Services LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA209726
Dosage form / routeTABLET · ORAL
Active ingredientsDIPHENHYDRAMINE HYDROCHLORIDE (25 mg/1)
NAPROXEN SODIUM (220 mg/1)
Marketing started20190131
Marketing ended20270131
Package count1

External sources

Source: openFDA. Public-domain (CC0).