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ibuprofen

NDC 41250-604 · Meijer Distribution Inc

Generic nameIbuprofen
Dosage formTABLET, FILM 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

41250-604-62 — 1 BOTTLE in 1 CARTON (41250-604-62) / 24 TABLET, FILM COATED in 1 BOTTLE

41250-604-71 — 1 BOTTLE in 1 CARTON (41250-604-71) / 50 TABLET, FILM COATED in 1 BOTTLE

41250-604-78 — 1 BOTTLE in 1 CARTON (41250-604-78) / 100 TABLET, FILM COATED in 1 BOTTLE

41250-604-82 — 2 BOTTLE in 1 CARTON (41250-604-82) / 100 TABLET, FILM COATED in 1 BOTTLE

41250-604-90 — 500 TABLET, FILM COATED in 1 BOTTLE (41250-604-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

41226-716 — Acetaminophen, Ibuprofen, 41250-050 — diphenhydramine citrate, ibuprofen, 41250-158 — Ibuprofen, phenylephrine HCl, 41250-255 — Ibuprofen, 41250-285 — IBUPROFEN, DIPHENHYDRAMINE HCL, 41250-286 — Ibuprofen, 41250-292 — Ibuprofen, 41250-293 — Ibuprofen, 41250-331 — ibuprofen, 41250-419 — Ibuprofen, 41250-647 — Ibuprofen, 41250-660 — Ibuprofen, 41250-685 — Ibuprofen, 41250-726 — ibuprofen, 41250-897 — Ibuprofen, 41250-991 — Ibuprofen, 41250-993 — Ibuprofen, 41520-050 — diphenhydramine citrate and ibuprofen, 41520-166 — Ibuprofen, 41520-255 — 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.