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Ibuprofen

NDC 59726-046 · P & L Development, LLC

Generic nameIbuprofen
Dosage formCAPSULE, LIQUID FILLED
RouteORAL
Active ingredient(s)IBUPROFEN
Strength200 mg/1
Pharmacologic classAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
Marketing categoryANDA

Packages

59726-046-16 — 160 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (59726-046-16)

59726-046-20 — 1 BOTTLE, PLASTIC in 1 BOX (59726-046-20) / 20 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC

59726-046-30 — 1 BOTTLE, PLASTIC in 1 BOX (59726-046-30) / 30 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

59556-857 — IBUPROFEN, 59556-858 — IBUPROFEN, 59556-895 — IBUPROFEN, 59640-020 — IBUPROFEN, DIPHENHYDRAMINE HCL, 59651-032 — Ibuprofen Oral, 59651-360 — Ibuprofen, 59651-361 — Ibuprofen, 59651-362 — Ibuprofen, 59651-908 — Ibuprofen and famotidine, 59726-003 — Ibuprofen, 59726-123 — Ibuprofen, 59726-139 — Ibuprofen, 59726-279 — Ibuprofen, 59726-745 — Ibuprofen, 59726-843 — Ibuprofen, 59779-050 — diphenhydramine citrate and ibuprofen, 59779-166 — Ibuprofen, 59779-291 — Ibuprofen, 59779-313 — Ibuprofen, 59779-430 — Ibuprofen and Pseudoephedrine Hydrochloride, +1311 more

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