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Butalbital, Acetaminophen, Caffeine

NDC 69367-203 · Westminster Pharmaceuticals, LLC

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

69367-203-01 — 100 TABLET in 1 BOTTLE (69367-203-01)

69367-203-05 — 500 TABLET in 1 BOTTLE (69367-203-05)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

69238-1993 — BUTALBITAL, ASPIRIN, CAFFEINE and CODEINE PHOSPHATE, 69256-343 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate, 69256-344 — Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate, 69256-466 — Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, 69256-898 — Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, 69256-899 — Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, 69292-301 — butalbital and acetaminophen, 69292-302 — butalbital and acetaminophen, 69292-303 — butalbital and acetaminophen, 69292-305 — butalbital, acetaminophen and caffeine, 69367-323 — Acetaminophen, 69367-416 — BUTALBITAL, ASPIRIN, AND CAFFEINE, 69396-140 — Acetaminophen, 69396-144 — Acetaminophen, 69423-759 — Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl, 69423-788 — Acetaminophen, Dextromethorphan Hydrobromide, and Phenylephrine Hydrochloride, 69423-789 — Acetaminophen, Dextromethorphan Hydrobromide, and Doxylamine succinate, 69423-791 — Acetaminophen, Dextromethorphan Hydrobromide, and Doxylamine succinate, 69423-800 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 69423-801 — Acetaminophen, Dextromethorphan HBr, 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.