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Butalbital And Acetaminophen

NDC 68047-721 · Larken Laboratories, Inc.

Generic namebutalbital and acetaminophen
Dosage formTABLET
RouteORAL
Active ingredient(s)BUTALBITAL, ACETAMINOPHEN
Strength325; 50 mg/1; mg/1
Pharmacologic classBarbiturate [EPC], Barbiturates [CS]
DEA scheduleCIII
Marketing categoryANDA

Packages

68047-721-01 — 100 TABLET in 1 BOTTLE (68047-721-01)

68047-721-30 — 30 TABLET in 1 BOTTLE (68047-721-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68001-495 — Acetaminophen, 68016-154 — ACETAMINOPHEN, DIPHENHYDRAMINE HCL, PHENYLEPHRINE HCL, 68016-198 — Acetaminophen, 68016-303 — Acetaminophen, 68016-543 — Acetaminophen, 68016-654 — Acetaminophen Diphenhydramine HCl, 68016-734 — Acetaminophen, 68016-797 — Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, 68016-877 — Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, 68016-878 — Acetaminophen, Dextromethorphan HBr and Doxylamine Succinate, 68047-752 — butalbital and acetaminophen, 68047-753 — butalbital and acetaminophen, 68071-2494 — Hydrocodone Bitartrate and Acetaminophen, 68071-2645 — Hydrocodone Bitartrate and Acetaminophen, 68071-3249 — Butalbital, Acetaminophen, and Caffeine, 68071-3437 — Acetaminophen, 68071-3447 — Hydrocodone Bitartrate and Acetaminophen, 68071-3454 — Acetaminophen, 68071-3565 — Acetaminophen, 68071-3651 — acetaminophen and codeine phosphate, +3486 more

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