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IBUPROFEN CA

NDC 11673-990 · TARGET CORPORATION

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

11673-990-20 — 200 TABLET, COATED in 1 BOTTLE (11673-990-20)

11673-990-42 — 24 TABLET, COATED in 1 BOTTLE (11673-990-42)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

11673-166 — Ibuprofen, 11673-225 — IBUPROFEN, DIPHENHYDRAMINE HCL, 11673-255 — Ibuprofen, 11673-593 — ibuprofen, 11673-604 — Ibuprofen, 11673-660 — Ibuprofen, 11673-683 — Ibuprofen Mini 200 mg, 11673-685 — Ibuprofen, 11673-741 — ibuprofen, 11673-924 — Acetaminophen, Ibuprofen, 11673-991 — IBUPROFEN, 11673-992 — IBUPROFEN, 11673-993 — IBUPROFEN, 11788-008 — Ibuprofen, 11788-009 — Ibuprofen, 11788-010 — Ibuprofen, 11822-0050 — Diphenhydramine Citrate, Ibuprofen, 11822-0084 — Ibuprofen and Pseudoephedrine Hydrochloride, 11822-0166 — Ibuprofen, 11822-0231 — 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.