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CareOne Ibuprofen

NDC 41520-495 · American Sales Company

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

41520-495-71 — 1 BOTTLE in 1 CARTON (41520-495-71) / 50 TABLET, FILM COATED in 1 BOTTLE

41520-495-78 — 1 BOTTLE in 1 CARTON (41520-495-78) / 100 TABLET, FILM COATED in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 41520-604 — Ibuprofen, 41520-633 — ibuprofen, 41520-647 — Ibuprofen, 41520-685 — Ibuprofen, 41520-740 — ibuprofen, 41520-745 — Ibuprofen, 41520-897 — Ibuprofen, 42507-050 — diphenhydramine citrate, ibuprofen, 42507-057 — ibuprofen, 42507-112 — 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.