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Ibuprofen

NDC 41163-509 · United Natural Foods, Inc. dba UNFI

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 categoryANDA

Packages

41163-509-06 — 1000 TABLET, COATED in 1 BOTTLE, PLASTIC (41163-509-06)

41163-509-17 — 150 TABLET, COATED in 1 BOTTLE, PLASTIC (41163-509-17)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

37835-588 — Ibuprofen, 41163-050 — diphenhydramine citrate, ibuprofen, 41163-057 — ibuprofen, 41163-103 — Acetaminophen, Ibuprofen, 41163-116 — Ibuprofen, 41163-158 — Ibuprofen, phenylephrine HCl, 41163-166 — Ibuprofen, 41163-185 — Ibuprofen, 41163-255 — Ibuprofen, 41163-312 — Ibuprofen, 41163-604 — Ibuprofen, 41163-647 — Ibuprofen, 41163-685 — Ibuprofen, 41163-710 — ibuprofen, 41163-897 — Ibuprofen, 41226-600 — IBUPROFEN, 41226-601 — IBUPROFEN, 41226-610 — IBUPROFEN, 41226-612 — Ibuprofen Tablets USP, 200mg, 41226-700 — 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.