migraine formula

NDC 42507-374 · HyVee 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

42507-374-62 — 1 BOTTLE in 1 CARTON (42507-374-62) / 24 TABLET, FILM COATED in 1 BOTTLE (42507-374-24)

42507-374-78 — 1 BOTTLE in 1 CARTON (42507-374-78) / 100 TABLET, FILM COATED in 1 BOTTLE (42507-374-00)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

42507-163 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 42507-170 — Acetaminophen, 42507-173 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 42507-205 — Acetaminophen, 42507-219 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 42507-223 — ACETAMINOPHEN and PHENYLEPHRINE HYDROCHLORIDE, 42507-274 — Aspirin, 42507-278 — ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 42507-303 — Acetaminophen, 42507-320 — ACETAMINOPHEN and PHENYLEPHRINE HYDROCHLORIDE, 42507-375 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 42507-401 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 42507-404 — Acetaminophen, 42507-437 — Acetaminophen, Diphenhydramine HCl, 42507-467 — Aspirin, 42507-484 — Acetaminophen, 42507-501 — Acetaminophen, 42507-511 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 42507-522 — acetaminophen, dextromethorphan Hbr, Phenylephrine HCl, 42507-532 — acetaminophen, dextromethorphan hydrobromide, +4118 more

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