ADVIL

NDC 0573-0166 · Haleon US Holdings LLC

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

0573-0166-51 — 1 BOTTLE in 1 CARTON (0573-0166-51) / 200 TABLET, COATED in 1 BOTTLE

0573-0166-85 — 225 TABLET, COATED in 1 BOTTLE (0573-0166-85)

FDA lists these products with the same active ingredient.

0573-0147 — Ibuprofen, Acetaminophen, 0573-0148 — diphenhydramine HCl, ibuprofen, 0573-0149 — ibuprofen, 0573-0150 — ibuprofen, 0573-0151 — ibuprofen, 0573-0154 — ibuprofen, 0573-0160 — ibuprofen, 0573-0161 — ibuprofen, 0573-0164 — diphenhydramine citrate and ibuprofen, 0573-0165 — ibuprofen, 0573-0167 — diphenhydramine HCl, ibuprofen, 0573-0168 — ibuprofen, 0573-0169 — ibuprofen, 0573-0170 — ibuprofen, 0573-0171 — ibuprofen, 0573-0174 — ibuprofen, 0573-0175 — ibuprofen, 0573-0179 — ibuprofen, 0573-0180 — ibuprofen and pseudoephedrine hydrochloride, 0573-0184 — ibuprofen, pseudoephedrine hydrochloride, +1312 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.