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Ibuprofen PM

NDC 21130-056 · HUMAN OTC DRUG · TABLET, COATED

Generic nameDiphenhydramine Citrate, Ibuprofen
Labeler / ManufacturerSafeway, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA211404
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsDIPHENHYDRAMINE CITRATE (38 mg/1)
IBUPROFEN (200 mg/1)
Marketing started20240301
Marketing ended20261231
Package count2

External sources

Source: openFDA. Public-domain (CC0).