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Ibuprofen

NDC 63868-979 · CHAIN DRUG MARKETING ASSOCIATION 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

63868-979-10 — 1 BOTTLE, PLASTIC in 1 CARTON (63868-979-10) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

63868-979-24 — 1 BOTTLE, PLASTIC in 1 CARTON (63868-979-24) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

63868-979-50 — 1 BOTTLE, PLASTIC in 1 CARTON (63868-979-50) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

63868-268 — Ibuprofen, 63868-427 — Ibuprofen, 63868-428 — Ibuprofen, 63868-470 — Ibuprofen, 63868-570 — Ibuprofen, 63868-571 — Ibuprofen, 63868-773 — Ibuprofen, 63868-796 — IBUPROFEN, 63868-805 — Ibuprofen, 63868-829 — IBUPROFEN, DIPHENHYDRAMINE HCL, 63941-109 — Ibuprofen, 63941-111 — Ibuprofen, 63941-127 — IBUPROFEN, 63941-128 — IBUPROFEN, 63941-209 — Ibuprofen, 63941-210 — Ibuprofen, 63941-301 — Ibuprofen, 63941-680 — Ibuprofen, 63941-682 — IBUPROFEN, DIPHENHYDRAMINE HCL, 63941-745 — 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.