migraine formula

NDC 41250-374 · Meijer Distribution Inc

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

41250-374-62 — 1 BOTTLE in 1 CARTON (41250-374-62) / 24 TABLET, FILM COATED in 1 BOTTLE

41250-374-71 — 1 BOTTLE in 1 CARTON (41250-374-71) / 50 TABLET, FILM COATED in 1 BOTTLE

41250-374-78 — 1 BOTTLE in 1 CARTON (41250-374-78) / 100 TABLET, FILM COATED in 1 BOTTLE

41250-374-82 — 1 BOTTLE in 1 CARTON (41250-374-82) / 200 TABLET, FILM COATED in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

41250-195 — Acetaminophen and Diphenhydramine Hydrochloride, 41250-197 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 41250-219 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 41250-222 — Aspirin, Citric Acid, Sodium Bicarbonate, 41250-244 — Acetaminophen, 41250-246 — Acetaminophen, 41250-274 — Aspirin, 41250-275 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 41250-334 — Acetaminophen, Aspirin, Caffeine, 41250-335 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 41250-403 — Acetaminophen, 41250-459 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 41250-467 — Aspirin, 41250-484 — Acetaminophen, 41250-501 — Acetaminophen, 41250-554 — Acetaminophen, 41250-570 — Acetaminophen, 41250-574 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 41250-590 — acetaminophen, 41250-600 — Aspirin, +4118 more

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