Skip to main content

Ibuprofen

NDC 0472-2002 · Actavis Pharma, Inc.

Generic nameIbuprofen
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

0472-2002-16 — 473 mL in 1 BOTTLE (0472-2002-16)

0472-2002-94 — 1 BOTTLE in 1 CARTON (0472-2002-94) / 118 mL in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0363-8574 — Ibuprofen, 0363-8901 — Ibuprofen, 0363-9131 — Acetaminophen and Ibuprofen, 0363-9593 — Ibuprofen, 0363-9594 — IBUPROFEN, 0363-9600 — IBUPROFEN, 0363-9601 — IBUPROFEN, 0363-9611 — IBUPROFEN, 0363-9612 — IBUPROFEN, 0404-0017 — Ibuprofen, 0536-1147 — Ibuprofen, 0536-1376 — Acetaminophen and Ibuprofen, 0573-0145 — Ibuprofen, Acetaminophen, 0573-0147 — Ibuprofen, Acetaminophen, 0573-0148 — diphenhydramine HCl, ibuprofen, 0573-0149 — ibuprofen, 0573-0150 — ibuprofen, 0573-0151 — ibuprofen, 0573-0154 — ibuprofen, 0573-0160 — 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.