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Ibuprofen

NDC 70518-3178 · REMEDYREPACK INC.

Generic nameIbuprofen
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)IBUPROFEN
Strength800 mg/1
Pharmacologic classAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
Marketing categoryANDA

Packages

70518-3178-0 — 15 TABLET, FILM COATED in 1 BLISTER PACK (70518-3178-0)

70518-3178-1 — 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3178-1)

70518-3178-3 — 45 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3178-3)

70518-3178-5 — 27 TABLET, FILM COATED in 1 BLISTER PACK (70518-3178-5)

70518-3178-6 — 100 POUCH in 1 BOX (70518-3178-6) / 1 TABLET, FILM COATED in 1 POUCH (70518-3178-7)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70264-044 — Ibuprofen, 70512-780 — ibuprofen, 70512-794 — ibuprofen, 70518-0176 — Ibuprofen, 70518-0761 — Ibuprofen, 70518-1051 — Ibuprofen, 70518-1364 — Ibuprofen, 70518-1409 — Ibuprofen, 70518-2432 — Ibuprofen, 70518-2902 — 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, 70677-0150 — Ibuprofen Oral, 70677-0151 — Ibuprofen Oral, +1311 more

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