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Ibuprofen

NDC 71205-716 · Proficient Rx LP

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

71205-716-72 — 1 BOTTLE in 1 CARTON (71205-716-72) / 120 mL in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71141-114 — Ibuprofen, 71141-178 — Ibuprofen, 71205-213 — Ibuprofen, 71205-357 — Ibuprofen, 71205-367 — Ibuprofen, 71205-395 — Ibuprofen, 71205-425 — ibuprofen, 71205-464 — Ibuprofen, 71205-522 — Ibuprofen, 71205-604 — Ibuprofen, 71205-787 — Ibuprofen, 71335-0690 — Ibuprofen, 71335-1073 — Ibuprofen, 71335-1206 — Ibuprofen, 71335-1207 — Ibuprofen, 71335-1218 — Ibuprofen, 71335-1270 — Ibuprofen, 71335-1396 — IBUPROFEN, 71335-1503 — IBUPROFEN, 71335-1517 — 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.

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels