IBUPROFEN, DIPHENHYDRAMINE HCL

NDC 69452-205 · Bionpharma Inc.

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

69452-205-04 — 1 BLISTER PACK in 1 CARTON (69452-205-04) / 6 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

69452-205-11 — 20 CAPSULE, LIQUID FILLED in 1 BOTTLE (69452-205-11)

69452-205-15 — 40 CAPSULE, LIQUID FILLED in 1 BOTTLE (69452-205-15)

69452-205-20 — 100 CAPSULE, LIQUID FILLED in 1 BOTTLE (69452-205-20)

69452-205-78 — 80 CAPSULE, LIQUID FILLED in 1 BOTTLE (69452-205-78)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

69396-025 — Diphenhydramine hydrochloride 2%, zinc acetate 0.1%, 69396-141 — Ibuprofen, 69396-145 — Ibuprofen, 69396-150 — Diphenhydramine hydrochloride 2%, zinc acetate 0.1%, 69396-172 — Ibuprofen, 69423-795 — Diphenhydramine Hydrochloride, 69423-812 — Diphenhydramine HCl, 69423-830 — Diphenhydramine HCl, 69423-834 — Acetaminophen, Diphenhydramine HCl, 69423-985 — Diphenhydramine Hydrochloride and Acetaminophen, 69452-212 — Ibuprofen, 69452-239 — Ibuprofen, 69452-260 — Ibuprofen, 69452-262 — Ibuprofen, 69452-263 — Ibuprofen, 69452-264 — IBUPROFEN, DIPHENHYDRAMINE HCL, 69452-302 — Ibuprofen, 69452-305 — Ibuprofen, 69452-322 — Diphenhydramine HCl, 69452-376 — Itch Relief Gel, +2338 more

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