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dual pain reliever

NDC 0363-5220 · Walgreen Company

Generic nameAcetaminophen, Ibuprofen
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)ACETAMINOPHEN, IBUPROFEN
Strength250; 125 mg/1; mg/1
Pharmacologic classAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
Marketing categoryANDA

Packages

0363-5220-01 — 1 BOTTLE in 1 CARTON (0363-5220-01) / 216 TABLET, FILM COATED in 1 BOTTLE

0363-5220-16 — 1 BOTTLE in 1 CARTON (0363-5220-16) / 144 TABLET, FILM COATED in 1 BOTTLE

0363-5220-23 — 1 BOTTLE in 1 CARTON (0363-5220-23) / 72 TABLET, FILM COATED in 1 BOTTLE

0363-5220-68 — 1 BOTTLE in 1 CARTON (0363-5220-68) / 36 TABLET, FILM COATED in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0363-3909 — Acetaminophen, Caffeine, Pyrilamine maleate, 0363-4050 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 0363-4066 — Acetaminophen, Phenylephrine HCl, 0363-4081 — Acetaminophen and Ibuprofen, 0363-4150 — Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride, 0363-4381 — Ibuprofen, 0363-5001 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 0363-5027 — Acetaminophen, Guaifenesin, Phenylephrine HCl, 0363-5100 — Ibuprofen, 0363-5101 — Acetaminophen, 0363-5309 — Acetaminophen, Dextromethorphan HBr, 0363-5410 — ACETAMINOPHEN, DIPHENHYDRAMINE, PHENYLEPHRINE, 0363-5430 — ACETAMINOPHEN, DIPHENHYDRAMINE HCl, PHENYLEPHRINE HCl, 0363-5470 — ACETAMINOPHEN, DEXTROMETHORPHAN HBr, PHENYLEPHRINE HCl, 0363-6002 — acetaminophen, 0363-6020 — acetaminophen, 0363-6028 — Acetaminophen, Guaifenesin, Phenylephrine HCl, 0363-6142 — acetaminophen, dextromethorphan HBr, doxylamine succinate, and phenylephrine hydrochloride, 0363-6150 — Acetaminophen, Guaifenesin, Phenylephrine HCl, 0363-6171 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, +4731 more

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