Motrin IB

NDC 67751-120 · Navajo Manufacturing Company Inc.

Generic nameIBUPROFEN

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)IBUPROFEN

Strength200 mg/1

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

Marketing categoryNDA

Packages

67751-120-01 — 1 POUCH in 1 CARTON (67751-120-01) / 2 TABLET, FILM COATED in 1 POUCH

67751-120-02 — 2 POUCH in 1 CARTON (67751-120-02) / 2 TABLET, FILM COATED in 1 POUCH

FDA lists these products with the same active ingredient.

67091-185 — Ibuprofen, 67091-347 — Ibuprofen, 67091-348 — Ibuprofen, 67091-368 — Ibuprofen, 67091-369 — Ibuprofen, 67296-0913 — IBU, 67296-2181 — Ibuprofen, 67296-2184 — Ibuprofen, 67296-2196 — Ibuprofen, 67414-240 — 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, 67877-320 — Ibuprofen, 67877-321 — Ibuprofen, 67877-626 — Ibuprofen and famotidine, +1312 more

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