Ibuprofen

NDC 0904-5309 · Major Pharmaceuticals

Generic nameIbuprofen

Dosage formSUSPENSION

RouteORAL

Active ingredient(s)IBUPROFEN

Strength100 mg/5mL

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

Marketing categoryANDA

Packages

0904-5309-09 — 1 BOTTLE in 1 CARTON (0904-5309-09) / 240 mL in 1 BOTTLE

0904-5309-20 — 1 BOTTLE in 1 CARTON (0904-5309-20) / 120 mL in 1 BOTTLE

FDA lists these products with the same active ingredient.

0573-0290 — ibuprofen, 0573-1174 — ibuprofen, 0573-1711 — ibuprofen, 0573-1769 — ibuprofen, 0573-2160 — ibuprofen and pseudoephedrine hydrochloride, 0573-2161 — chlorpheniramine maleate, ibuprofen, and phenylephrine hydrochloride, 0615-8309 — Ibuprofen, 0615-8310 — IBUPROFEN, 0615-8311 — Ibuprofen, 0761-0908 — IBUPROFEN, 0904-5463 — ibuprofen, 0904-5577 — Ibuprofen, 0904-5853 — Ibuprofen, 0904-5854 — Ibuprofen, 0904-5855 — Ibuprofen, 0904-6747 — Ibuprofen, 0904-7587 — Ibuprofen, 0904-7588 — Ibuprofen, 0904-7592 — Ibuprofen, 0904-7912 — 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.