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IBUPROFEN

NDC 67060-001 · ADVANCED FIRST AID, INC.

Generic nameIBUPROFEN 200MG
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

67060-001-67 — 250 PACKET in 1 CARTON (67060-001-67) / 2 TABLET, FILM COATED in 1 PACKET

67060-001-68 — 100 PACKET in 1 CARTON (67060-001-68) / 2 TABLET, FILM COATED in 1 PACKET

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

66715-9633 — Ibuprofen and Diphenhydramine citrate, 66715-9700 — Ibuprofen, 66715-9733 — Ibuprofen and Diphenhydramine citrate, 66715-9752 — Ibuprofen, 66715-9812 — Ibuprofen, 66715-9819 — Ibuprofen tablet, film-coated, 66715-9839 — Ibuprofen, 67046-1214 — Ibuprofen, 67046-1606 — Ibuprofen, 67046-1646 — Ibuprofen, 67091-185 — Ibuprofen, 67091-347 — Ibuprofen, 67091-348 — Ibuprofen, 67091-368 — Ibuprofen, 67091-369 — Ibuprofen, 67296-0913 — IBU, 67296-2181 — Ibuprofen, 67296-2184 — Ibuprofen, 67296-2196 — Ibuprofen, 67414-240 — 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.