Ibuprofen

NDC 67296-2184 · Redpharm Drug

FDA carries 2 listing records for this NDC; the most recent is shown.

Generic nameIbuprofen

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)IBUPROFEN

Strength400 mg/1

Pharmacologic classAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]

Marketing categoryANDA

Packages

67296-2184-3 — 30 TABLET, FILM COATED in 1 BOTTLE (67296-2184-3)

67296-2184-2 — 20 TABLET, FILM COATED in 1 BOTTLE (67296-2184-2)

FDA lists these products with the same active ingredient.

67046-1606 — Ibuprofen, 67046-1646 — Ibuprofen, 67060-001 — IBUPROFEN 200MG, 67091-185 — Ibuprofen, 67091-347 — Ibuprofen, 67091-348 — Ibuprofen, 67091-368 — Ibuprofen, 67091-369 — Ibuprofen, 67296-0913 — IBU, 67296-2181 — Ibuprofen, 67296-2196 — Ibuprofen, 67414-240 — IBUPROFEN, 67751-120 — IBUPROFEN, 67751-146 — IBUPROFEN, 67751-147 — DIPHENHYDRAMINE CITRATE, IBUPROFEN, 67751-148 — IBUPROFEN, 67751-149 — CHLORPHENIRAMINE MALEATE, IBUPROFEN, PHENYLEPHRINE HYDROCHLORIDE, 67751-150 — IBUPROFEN, PHENYLEPHRINE HYDROCHLORIDE, 67751-211 — Ibuprofen, Acetaminophen, 67877-319 — Ibuprofen, +1312 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.