ibuprofen

NDC 10267-3846 · Contract Pharmacal Corp.

Generic nameibuprofen

Dosage formTABLET

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

10267-3846-2 — 250 TABLET in 1 BOTTLE (10267-3846-2)

FDA lists these products with the same active ingredient.

0904-6747 — Ibuprofen, 0904-7587 — 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, 10267-3852 — ibuprofen, 10267-3909 — ibuprofen, 11673-050 — diphenhydramine citrate and ibuprofen, 11673-166 — Ibuprofen, 11673-225 — IBUPROFEN, DIPHENHYDRAMINE HCL, 11673-255 — Ibuprofen, 11673-593 — ibuprofen, 11673-604 — Ibuprofen, 11673-660 — Ibuprofen, 11673-683 — Ibuprofen Mini 200 mg, +1312 more

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