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Ibuprofen and Diphenhydramine Citrate

NDC 55111-565 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerDr. Reddy's Laboratories Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA090619
Dosage form / routeTABLET · ORAL
Active ingredientsDIPHENHYDRAMINE CITRATE (38 mg/1)
IBUPROFEN (200 mg/1)
Marketing started20100131
Package count8

External sources

Source: openFDA. Public-domain (CC0).