Ibuprofen

NDC 0904-7587 · Major Pharmaceuticals

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

0904-7587-40 — 500 TABLET, FILM COATED in 1 BOTTLE (0904-7587-40)

0904-7587-59 — 100 TABLET, FILM COATED in 1 BOTTLE (0904-7587-59)

FDA lists these products with the same active ingredient.

0615-8310 — IBUPROFEN, 0615-8311 — Ibuprofen, 0761-0908 — IBUPROFEN, 0904-5309 — Ibuprofen, 0904-5463 — ibuprofen, 0904-5577 — Ibuprofen, 0904-5853 — Ibuprofen, 0904-5854 — Ibuprofen, 0904-5855 — Ibuprofen, 0904-6747 — Ibuprofen, 0904-7588 — Ibuprofen, 0904-7592 — Ibuprofen, 0904-7912 — Ibuprofen, 0904-7914 — ibuprofen, 0924-0075 — Ibuprofen 200mg, 0924-0076 — Ibuprofen 200mg, 10202-150 — Ibuprofen, 10202-711 — Ibuprofen, 10267-3846 — ibuprofen, 10267-3852 — 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.