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Advil

NDC 66715-9700 · Lil' Drug Store Products, Inc.

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 categoryNDA

Packages

66715-9700-2 — 2 POUCH in 1 CARTON (66715-9700-2) / 2 TABLET, COATED in 1 POUCH

66715-9700-3 — 3 POUCH in 1 CARTON (66715-9700-3) / 2 TABLET, COATED in 1 POUCH

66715-9700-7 — 30 POUCH in 1 BOX, UNIT-DOSE (66715-9700-7) / 2 TABLET, COATED in 1 POUCH

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

66715-6512 — Ibuprofen, 66715-6533 — Ibuprofen and Diphenhydramine citrate, 66715-6552 — Ibuprofen, 66715-6720 — Ibuprofen, 66715-6739 — Ibuprofen, 66715-6839 — Ibuprofen, 66715-6920 — Ibuprofen, 66715-8152 — ibuprofen tablet, film coated, 66715-9601 — ibuprofen, acetaminophen tablet, film coated, 66715-9633 — Ibuprofen and Diphenhydramine citrate, 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, 67060-001 — IBUPROFEN 200MG, 67091-185 — 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.