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migraine relief

NDC 0363-1235 · Walgreen Company

Generic nameacetaminophen, aspirin, caffeine
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)ACETAMINOPHEN, ASPIRIN, CAFFEINE
Strength250; 250; 65 mg/1; mg/1; mg/1
Pharmacologic classAnti-Inflammatory Agents, Non-Steroidal [CS], Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE], Cyclooxygenase Inhibitors [MoA], Decreased Platelet Aggregation [PE], Decreased Prostaglandin Production [PE], Methylxanthine [EPC], Nonsteroidal Anti-inflammatory Drug [EPC], Platelet Aggregation Inhibitor [EPC], Xanthines [CS]
Marketing categoryANDA

Packages

0363-1235-27 — 1 BOTTLE in 1 CARTON (0363-1235-27) / 80 TABLET, FILM COATED in 1 BOTTLE

0363-1235-60 — 1 BOTTLE in 1 CARTON (0363-1235-60) / 20 TABLET, FILM COATED in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0363-0853 — Acetaminophine Dextromethorphan HBr Phenylphrine HCl, 0363-0863 — Acetaminophen, Diphenhydramine HCL, 0363-0865 — Acetaminophen, Aspirin, Caffeine, 0363-0875 — Aspirin, Chlorpheniramine Maleate, Phenylephrine Bitartrate, 0363-0886 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 0363-0892 — Acetaminophen, 0363-1011 — ACETAMINOPHEN, DEXTROMETHORPHAN HBr, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HCl, 0363-1137 — Acetaminophen, 0363-1150 — Acetaminophen, Aspirin, Caffeine, 0363-1178 — Acetaminophen, 0363-1239 — Acetaminophen, 0363-1320 — Acetaminophen 250mg Aspirin 250mg Caffeine 65mg, 0363-1502 — acetaminophen, 0363-1630 — Acetaminophen, 0363-1750 — Acetaminophen, 0363-1756 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate softgels, 0363-2029 — acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, phenylephrine hydrochloride, 0363-2035 — Acetaminophen, Diphenhydramine HCl, 0363-2310 — Acetaminophen 500mg Caffeine 60mg Pyrilamine maleate 15mg, 0363-3361 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, +4118 more

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