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Ibuprofen

NDC 53943-292 · Discount Drug Mart

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

53943-292-12 — 1 BOTTLE, PLASTIC in 1 CARTON (53943-292-12) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

53943-292-14 — 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53943-292-14)

53943-292-15 — 1 BOTTLE, PLASTIC in 1 CARTON (53943-292-15) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

53746-466 — Ibuprofen, 53942-112 — Ibuprofen, 53942-119 — IBUPROFEN, 53943-034 — Acetaminophen and Ibuprofen, 53943-111 — Ibuprofen, 53943-112 — Ibuprofen, 53943-119 — IBUPROFEN, 53943-212 — Ibuprofen, 53943-214 — Ibuprofen, 53943-291 — Ibuprofen, 53943-637 — Ibuprofen, 53943-682 — Ibuprofen, 54162-941 — Ibuprofen, 54348-825 — IBUPROFEN, 54348-830 — IBUPROFEN, 54348-835 — IBUPROFEN, 54473-306 — Ibuprofen, 55111-565 — Ibuprofen and Diphenhydramine Citrate, 55111-682 — Ibuprofen, 55111-683 — 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.