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good sense migraine formula

NDC 0113-0374 · L. Perrigo 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

0113-0374-62 — 1 BOTTLE in 1 CARTON (0113-0374-62) / 24 TABLET, FILM COATED in 1 BOTTLE

0113-0374-78 — 1 BOTTLE in 1 CARTON (0113-0374-78) / 100 TABLET, FILM COATED in 1 BOTTLE

0113-0374-82 — 1 BOTTLE in 1 CARTON (0113-0374-82) / 200 TABLET, FILM COATED in 1 BOTTLE (0113-0374-00)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0067-8212 — ACETAMINOPHEN, DIPHENHYDRAMINE HCl, PHENYLEPHRINE HCl, 0113-0019 — Acetaminophen, dextromethorphan HBr, doxylamine succinate, phenylephrine HCl, 0113-0020 — Acetaminophen, 0113-0025 — Acetaminophen, 0113-0044 — Acetaminophen, 0113-0056 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 0113-0161 — Acetaminophen, 0113-0212 — Acetaminophen, 0113-0274 — Aspirin, 0113-0335 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 0113-0403 — Acetaminophen, 0113-0437 — Acetaminophen, Diphenhydramine HCl, 0113-0459 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 0113-0467 — Aspirin, 0113-0484 — Acetaminophen, 0113-0544 — Acetaminophen, 0113-0603 — acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl, 0113-0608 — Acetaminophen, 0113-0656 — acetaminophen, dextromethorphan Hbr, Phenylephrine HCl, 0113-0763 — Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, 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.