Ibuprofen
NDC 59651-361 · Aurobindo Pharma Limited
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
59651-361-01 — 100 TABLET in 1 BOTTLE (59651-361-01)
59651-361-05 — 500 TABLET in 1 BOTTLE (59651-361-05)
Related Codes
Same active ingredient
FDA lists these products with the same active ingredient.
58602-902 — Ibuprofen, 59556-764 — IBUPROFEN, 59556-855 — Ibuprofen, 59556-856 — Ibuprofen, 59556-857 — IBUPROFEN, 59556-858 — IBUPROFEN, 59556-895 — IBUPROFEN, 59640-020 — IBUPROFEN, DIPHENHYDRAMINE HCL, 59651-032 — Ibuprofen Oral, 59651-360 — Ibuprofen, 59651-362 — Ibuprofen, 59651-908 — Ibuprofen and famotidine, 59726-003 — Ibuprofen, 59726-046 — Ibuprofen, 59726-123 — Ibuprofen, 59726-139 — Ibuprofen, 59726-279 — Ibuprofen, 59726-745 — Ibuprofen, 59726-843 — Ibuprofen, 59779-050 — diphenhydramine citrate and ibuprofen, +1311 more