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Ibuprofen 200 mg

NDC 70264-041 · R J General Corporation

Generic nameIbuprofen
Dosage formTABLET, 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 categoryOTC MONOGRAPH DRUG

Packages

70264-041-01 — 25 POUCH in 1 CARTON (70264-041-01) / 2 TABLET, COATED in 1 POUCH

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70000-0622 — Acetaminophen and Ibuprofen, 70000-0737 — Acetaminophen, Ibuprofen, 70010-066 — Ibuprofen, 70010-067 — Ibuprofen, 70010-068 — Ibuprofen, 70010-131 — Acetaminophen and Ibuprofen, 70010-213 — Acetaminophen and Ibuprofen, 70038-131 — Acetaminophen, 70264-029 — IBUPROFEN, 70264-040 — Acetaminophen 250 mg and Ibuprofen 125 mg, 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, +1311 more

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