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Ibuprofen

NDC 70518-0761 · REMEDYREPACK 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

70518-0761-0 — 20 TABLET, FILM COATED in 1 BLISTER PACK (70518-0761-0)

70518-0761-1 — 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0761-1)

70518-0761-2 — 28 TABLET, FILM COATED in 1 BLISTER PACK (70518-0761-2)

70518-0761-3 — 21 TABLET, FILM COATED in 1 BLISTER PACK (70518-0761-3)

70518-0761-4 — 15 TABLET, FILM COATED in 1 BLISTER PACK (70518-0761-4)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70038-131 — Acetaminophen, 70264-029 — IBUPROFEN, 70264-040 — Acetaminophen 250 mg and Ibuprofen 125 mg, 70264-041 — Ibuprofen, 70264-042 — Ibuprofen, 70264-043 — Ibuprofen, 70264-044 — Ibuprofen, 70512-780 — ibuprofen, 70512-794 — ibuprofen, 70518-0176 — Ibuprofen, 70518-1051 — Ibuprofen, 70518-1364 — Ibuprofen, 70518-1409 — Ibuprofen, 70518-2432 — Ibuprofen, 70518-2902 — Ibuprofen, 70518-3178 — Ibuprofen, 70518-3313 — Ibuprofen, 70518-3861 — Ibuprofen, 70518-4010 — Ibuprofen, 70518-4259 — Ibuprofen, +1311 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.