Skip to main content

ACETAMINOPHEN AND CODEINE PHOSPHATE

NDC 68788-7835 · Preferred Pharmaceuticals Inc.

Generic nameacetaminophen and codeine phosphate
Dosage formTABLET
RouteORAL
Active ingredient(s)ACETAMINOPHEN, CODEINE PHOSPHATE
Strength300; 30 mg/1; mg/1
Pharmacologic classFull Opioid Agonists [MoA], Opioid Agonist [EPC]
DEA scheduleCIII
Marketing categoryANDA

Packages

68788-7835-1 — 15 TABLET in 1 BOTTLE (68788-7835-1)

68788-7835-2 — 20 TABLET in 1 BOTTLE (68788-7835-2)

68788-7835-3 — 30 TABLET in 1 BOTTLE (68788-7835-3)

68788-7835-6 — 60 TABLET in 1 BOTTLE (68788-7835-6)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68391-659 — Acetaminophen, 68391-863 — Acetaminophen, Diphenhydramine HCL, 68599-4679 — Acetaminophen, 68599-4681 — Pain reliever, 68599-4751 — Acetaminophen, Phenylephrine HCl, 68682-306 — Butalbital and Acetaminophen tablets, 68788-4009 — ACETAMINOPHEN and IBUPROFEN, 68788-4065 — Acetaminophen, 68788-4126 — Butalbital, Acetaminophen and Caffeine, 68788-4132 — ACETAMINOPHEN, 68788-7855 — Tramadol Hydrochloride and Acetaminophen, 68788-7859 — acetaminophen and codeine phosphate, 68788-8137 — Butalbital, Acetaminophen, and Caffeine, 68788-8361 — Guaifenesin and Codeine Phosphate, 68788-8375 — Acetaminophen, 68788-8397 — Acetaminophen, 68788-8407 — Acetaminophen, 68788-8477 — Acetaminophen, 68788-8559 — Acetaminophen, 68788-8585 — Acetaminophen, +3502 more

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