Ibuprofen

NDC 65162-465 · Amneal Pharmaceuticals LLC

Generic nameIbuprofen

Dosage formTABLET

RouteORAL

Active ingredient(s)IBUPROFEN

Strength600 mg/1

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

Marketing categoryANDA

Packages

65162-465-03 — 30 TABLET in 1 BOTTLE (65162-465-03)

65162-465-05 — 50 TABLET in 1 BOTTLE (65162-465-05)

65162-465-06 — 60 TABLET in 1 BOTTLE (65162-465-06)

65162-465-09 — 90 TABLET in 1 BOTTLE (65162-465-09)

65162-465-10 — 100 TABLET in 1 BOTTLE (65162-465-10)

65162-465-50 — 500 TABLET in 1 BOTTLE (65162-465-50)

FDA lists these products with the same active ingredient.

63981-517 — Ibuprofen, 63981-598 — IBUPROFEN, 63981-604 — Ibuprofen, 63981-750 — Ibuprofen, 64380-807 — Ibuprofen, 64380-808 — Ibuprofen, 64380-809 — Ibuprofen, 64380-997 — Ibuprofen, 65162-356 — Ibuprofen, 65162-464 — Ibuprofen, 65162-466 — Ibuprofen, 65162-770 — Ibuprofen, 66220-284 — ibuprofen, 66220-287 — ibuprofen, 66267-115 — ibuprofen, 66267-963 — Ibuprofen, 66267-964 — Ibuprofen, 66715-5507 — Ibuprofen, 66715-5539 — Ibuprofen, 66715-5607 — 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.