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Butalbital and Acetaminophen

NDC 68682-306 · Oceanside Pharmaceuticals

Generic nameButalbital and Acetaminophen tablets
Dosage formTABLET
RouteORAL
Active ingredient(s)BUTALBITAL, ACETAMINOPHEN
Strength300; 50 mg/1; mg/1
Pharmacologic classBarbiturate [EPC], Barbiturates [CS]
DEA scheduleCIII
Marketing categoryANDA

Packages

68682-306-01 — 100 TABLET in 1 BOTTLE, PLASTIC (68682-306-01)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68210-5053 — Acetaminophen, Dextromethorphan Hydrobromide and Phenylephrine Hydrochloride, 68391-004 — Acetaminophen, 68391-288 — Acetaminophen, 68391-411 — Acetaminophen, 68391-430 — Acetaminophen, Diphenhydramine, 68391-659 — Acetaminophen, 68391-863 — Acetaminophen, Diphenhydramine HCL, 68599-4679 — Acetaminophen, 68599-4681 — Pain reliever, 68599-4751 — Acetaminophen, Phenylephrine HCl, 68788-4009 — ACETAMINOPHEN and IBUPROFEN, 68788-4065 — Acetaminophen, 68788-4126 — Butalbital, Acetaminophen and Caffeine, 68788-4132 — ACETAMINOPHEN, 68788-7835 — acetaminophen and codeine phosphate, 68788-7855 — Tramadol Hydrochloride and Acetaminophen, 68788-7859 — acetaminophen and codeine phosphate, 68788-8137 — Butalbital, Acetaminophen, and Caffeine, 68788-8375 — Acetaminophen, 68788-8397 — Acetaminophen, +3486 more

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