BUTALBITAL, ACETAMINOPHEN AND CAFFEINE

NDC 70518-4601 · REMEDYREPACK INC.

Generic nameBUTALBITAL, ACETAMINOPHEN AND CAFFEINE

Dosage formTABLET

RouteORAL

Active ingredient(s)BUTALBITAL, ACETAMINOPHEN, CAFFEINE

Strength325; 50; 40 mg/1; mg/1; mg/1

Pharmacologic classBarbiturate [EPC], Barbiturates [CS], Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE], Methylxanthine [EPC], Xanthines [CS]

DEA scheduleCIII

Marketing categoryANDA

Packages

70518-4601-0 — 90 TABLET in 1 BOTTLE, PLASTIC (70518-4601-0)

70518-4601-1 — 150 TABLET in 1 BOTTLE, PLASTIC (70518-4601-1)

70518-4601-2 — 120 TABLET in 1 BOTTLE, PLASTIC (70518-4601-2)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70264-047 — ACETAMINOPHEN, DEXTROMETHORPHAN HBr, 70518-1134 — Butalbital, Acetaminophen, and Caffeine, 70518-2628 — acetaminophen and codeine phosphate, 70518-2764 — acetaminophen and codeine phosphate, 70518-3705 — acetaminophen and codeine phosphate, 70518-4104 — Acetaminophen and Codeine Phosphate, 70518-4184 — Acetaminophen, 70518-4309 — Butalbital, Acetaminophen, and Caffeine, 70518-4461 — Tramadol Hydrochloride and Acetaminophen, 70518-4467 — Butalbital, Acetaminophen, and Caffeine, 70677-0081 — Acetaminophen, Diphenhydramine HCL, 70677-0117 — Acetaminophen, 70677-1004 — ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, and PHENYLEPHRINE HYDROCHLORIDE, 70677-1005 — ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE, 70677-1027 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 70677-1029 — acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, 70677-1030 — acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, phenylephrine hydrochloride, 70677-1031 — acetaminophen, dextromethorphan Hbr, Phenylephrine HCl, 70677-1032 — Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, 70677-1033 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine succinate, +3614 more

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