Ibuprofen

NDC 67091-348 · Winco Foods, LLC

Generic nameIbuprofen

Dosage formTABLET, 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 categoryANDA

Packages

67091-348-10 — 1 BOTTLE, PLASTIC in 1 CARTON (67091-348-10) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC

67091-348-50 — 1 BOTTLE, PLASTIC in 1 CARTON (67091-348-50) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC

FDA lists these products with the same active ingredient.

66715-9752 — Ibuprofen, 66715-9812 — Ibuprofen, 66715-9819 — Ibuprofen tablet, film-coated, 66715-9839 — Ibuprofen, 67046-1214 — Ibuprofen, 67046-1606 — Ibuprofen, 67046-1646 — Ibuprofen, 67060-001 — IBUPROFEN 200MG, 67091-185 — Ibuprofen, 67091-347 — Ibuprofen, 67091-368 — Ibuprofen, 67091-369 — Ibuprofen, 67296-0913 — IBU, 67296-2181 — Ibuprofen, 67296-2184 — Ibuprofen, 67296-2196 — Ibuprofen, 67414-240 — IBUPROFEN, 67751-120 — IBUPROFEN, 67751-146 — IBUPROFEN, 67751-147 — DIPHENHYDRAMINE CITRATE, 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.