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IBUPROFEN

NDC 72189-231 · DIRECT RX

Generic nameIBUPROFEN
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)IBUPROFEN
Strength600 mg/1
Pharmacologic classAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
Marketing categoryANDA

Packages

72189-231-21 — 21 TABLET, FILM COATED in 1 BOTTLE (72189-231-21)

72189-231-30 — 30 TABLET, FILM COATED in 1 BOTTLE (72189-231-30)

72189-231-60 — 60 TABLET, FILM COATED in 1 BOTTLE (72189-231-60)

72189-231-90 — 90 TABLET, FILM COATED in 1 BOTTLE (72189-231-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

72036-212 — Ibuprofen, 72090-070 — Ibuprofen, 72090-071 — Ibuprofen, 72162-1909 — Ibuprofen Oral, 72162-1910 — Ibuprofen Oral, 72162-1911 — Ibuprofen Oral, 72162-1912 — Ibuprofen Oral, 72162-2285 — Ibuprofen, 72162-2286 — Ibuprofen, 72162-2341 — Ibuprofen, 72189-266 — IBUPROFEN, 72189-324 — IBUPROFEN, 72189-556 — Ibuprofen, 72189-564 — Ibuprofen, 72189-641 — Ibuprofen Famotidine, 72189-643 — Ibuprofen, 72189-667 — Ibuprofen Famotidine, 72260-129 — ACETAMINOPHEN and IBUPROFEN, 72288-050 — diphenhydramine citrate, ibuprofen, 72288-057 — 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.