IBUPROFEN
NDC 68071-4459 · NuCare Pharmaceuticals,Inc.
Generic nameIBUPROFEN
Dosage formTABLET, FILM COATED
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
68071-4459-6 — 6 TABLET, FILM COATED in 1 BOTTLE (68071-4459-6)
Related Codes
Same active ingredient
FDA lists these products with the same active ingredient.
68071-3589 — Ibuprofen, 68071-3679 — Ibuprofen, 68071-3696 — Ibuprofen, 68071-3778 — Ibuprofen, 68071-3793 — Ibuprofen, 68071-3849 — Ibuprofen, 68071-3937 — Ibuprofen, 68071-3966 — Ibuprofen, 68071-4009 — IBUPROFEN, 68071-4243 — IBUPROFEN, 68071-4845 — Ibuprofen, 68071-4887 — Ibuprofen, 68071-4949 — Ibuprofen, 68071-4952 — Ibuprofen, 68071-4968 — Ibuprofen, 68071-5066 — Ibuprofen, 68071-5126 — IBUPROFEN, 68071-5134 — IBUPROFEN, 68071-5135 — IBUPROFEN, 68071-5140 — IBUPROFEN, +1311 more