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Ibuprofen

NDC 59651-032 · Aurobindo Pharma Limited

Generic nameIbuprofen Oral
Dosage formSUSPENSION
RouteORAL
Active ingredient(s)IBUPROFEN
Strength100 mg/5mL
Pharmacologic classAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
Marketing categoryANDA

Packages

59651-032-12 — 1 BOTTLE in 1 CARTON (59651-032-12) / 120 mL in 1 BOTTLE

59651-032-47 — 1 BOTTLE in 1 CARTON (59651-032-47) / 473 mL in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

58602-893 — Acetaminophen and Ibuprofen, 58602-895 — Acetaminophen and Ibuprofen, 58602-902 — Ibuprofen, 59556-764 — IBUPROFEN, 59556-855 — Ibuprofen, 59556-856 — Ibuprofen, 59556-857 — IBUPROFEN, 59556-858 — IBUPROFEN, 59556-895 — IBUPROFEN, 59640-020 — IBUPROFEN, DIPHENHYDRAMINE HCL, 59651-360 — Ibuprofen, 59651-361 — Ibuprofen, 59651-362 — Ibuprofen, 59651-908 — Ibuprofen and famotidine, 59726-003 — Ibuprofen, 59726-046 — Ibuprofen, 59726-123 — Ibuprofen, 59726-139 — Ibuprofen, 59726-279 — Ibuprofen, 59726-745 — 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.