Ibuprofen
NDC 70518-2432 · REMEDYREPACK INC.
Generic nameIbuprofen
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)IBUPROFEN
Strength400 mg/1
Pharmacologic classAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
Marketing categoryANDA
Packages
70518-2432-1 — 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2432-1)
Related Codes
Same active ingredient
FDA lists these products with the same active ingredient.
70264-042 — Ibuprofen, 70264-043 — Ibuprofen, 70264-044 — Ibuprofen, 70512-780 — ibuprofen, 70512-794 — ibuprofen, 70518-0176 — Ibuprofen, 70518-0761 — Ibuprofen, 70518-1051 — Ibuprofen, 70518-1364 — Ibuprofen, 70518-1409 — Ibuprofen, 70518-2902 — Ibuprofen, 70518-3178 — Ibuprofen, 70518-3313 — Ibuprofen, 70518-3861 — Ibuprofen, 70518-4010 — Ibuprofen, 70518-4259 — Ibuprofen, 70518-4341 — Ibuprofen, 70518-4580 — Ibuprofen and famotidine, 70518-4595 — Ibuprofen, 70677-0046 — Ibuprofen, +1311 more