Ibuprofen
NDC 55154-0669 · Cardinal Health 107, LLC
Generic nameIbuprofen
Dosage formTABLET, FILM COATED
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
55154-0669-0 — 10 BLISTER PACK in 1 BAG (55154-0669-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
Related Codes
Same active ingredient
FDA lists these products with the same active ingredient.
53943-682 — Ibuprofen, 54162-941 — Ibuprofen, 54348-825 — IBUPROFEN, 54348-830 — IBUPROFEN, 54348-835 — IBUPROFEN, 54473-306 — Ibuprofen, 55111-565 — Ibuprofen and Diphenhydramine Citrate, 55111-682 — Ibuprofen, 55111-683 — Ibuprofen, 55111-684 — Ibuprofen, 55154-0741 — Ibuprofen, 55154-1342 — Ibuprofen, 55154-1380 — Ibuprofen, 55154-1577 — Ibuprofen, 55154-2583 — Ibuprofen, 55301-050 — diphenhydramine citrate, ibuprofen, 55301-291 — Ibuprofen, 55301-292 — Ibuprofen, 55301-392 — Ibuprofen, 55301-393 — Ibuprofen, +1311 more