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up and up ibuprofen

NDC 11673-604 · Target Corporation

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

11673-604-78 — 1 BOTTLE in 1 CARTON (11673-604-78) / 100 TABLET, FILM COATED in 1 BOTTLE

11673-604-90 — 500 TABLET, FILM COATED in 1 BOTTLE (11673-604-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

10202-150 — Ibuprofen, 10202-711 — Ibuprofen, 10267-3846 — ibuprofen, 10267-3852 — ibuprofen, 10267-3909 — ibuprofen, 11673-050 — diphenhydramine citrate and ibuprofen, 11673-166 — Ibuprofen, 11673-225 — IBUPROFEN, DIPHENHYDRAMINE HCL, 11673-255 — Ibuprofen, 11673-593 — ibuprofen, 11673-660 — Ibuprofen, 11673-683 — Ibuprofen Mini 200 mg, 11673-685 — Ibuprofen, 11673-741 — ibuprofen, 11673-924 — Acetaminophen, Ibuprofen, 11673-990 — IBUPROFEN, 11673-991 — IBUPROFEN, 11673-992 — IBUPROFEN, 11673-993 — IBUPROFEN, 11788-008 — 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.