IBUPROFEN, DIPHENHYDRAMINE HCL

NDC 11673-225 · TARGET Corporation

Generic nameIBUPROFEN, DIPHENHYDRAMINE HCL

Dosage formCAPSULE, LIQUID FILLED

RouteORAL

Active ingredient(s)IBUPROFEN, DIPHENHYDRAMINE HYDROCHLORIDE

Strength25; 200 mg/1; mg/1

Pharmacologic classAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], Nonsteroidal Anti-inflammatory Drug [EPC]

Marketing categoryANDA

Packages

11673-225-15 — 1 BOTTLE in 1 CARTON (11673-225-15) / 40 CAPSULE, LIQUID FILLED in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

10267-3846 — ibuprofen, 10267-3852 — ibuprofen, 10267-3909 — ibuprofen, 11383-192 — Diphenhydramine Hydrochloride, Pramoxine Hydrochloride, 11527-069 — Anti Itch Cream, 11673-012 — Diphenhydramine HCl, 11673-050 — diphenhydramine citrate and ibuprofen, 11673-113 — Acetaminophen, Diphenhydramine hydrochloride, and Phenylephrine hydrochloride, 11673-166 — Ibuprofen, 11673-186 — diphenhydramine hydrochloride, 11673-255 — Ibuprofen, 11673-285 — Diphenhydramine Hydrochloride, 11673-360 — Diphenhydramine HCl, 11673-494 — Diphenhydramine HCl, 11673-496 — Diphenydramine Hydrochloride, 11673-593 — ibuprofen, 11673-604 — Ibuprofen, 11673-660 — Ibuprofen, 11673-683 — Ibuprofen Mini 200 mg, 11673-685 — Ibuprofen, +2338 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.