Skip to main content

ACETAMINOPHEN AND CODEINE

NDC 61919-484 · Direct_Rx

FDA carries 2 listing records for this NDC; the most recent is shown.

Generic nameACETAMINOPHEN AND CODEINE
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

61919-484-10 — 10 TABLET in 1 BOTTLE (61919-484-10)

61919-484-18 — 18 TABLET in 1 BOTTLE (61919-484-18)

61919-484-30 — 30 TABLET in 1 BOTTLE (61919-484-30)

61919-484-71 — 100 TABLET in 1 BOTTLE (61919-484-71)

61919-484-90 — 90 TABLET in 1 BOTTLE (61919-484-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

60760-965 — Oxycodone Hydrochloride and Acetaminophen, 60951-602 — Oxycodone and Acetaminophen, 60951-700 — Oxycodone and Acetaminophen, 60951-701 — Oxycodone and Acetaminophen, 60951-712 — Oxycodone and Acetaminophen, 61245-145 — Acetaminophen, 61245-175 — Acetaminophen, 61504-095 — Acetaminophen and Diphenhydramine Hydrochloride, 61504-104 — Acetaminophen, 61504-200 — Acetaminophen, 61919-871 — OXYCODONE AND ACETAMINOPHEN, 62011-0256 — Acetaminophen, Diphenhydramine HCl, 62011-0420 — Acetaminophen, Diphenhydramine HCL, 62011-0460 — Acetaminophen, 62011-0461 — Acetaminophen, 62135-751 — BUTALBITAL, ACETAMINOPHEN AND CAFFEINE, 62207-183 — ACETAMINOPHEN, 62207-188 — ACETAMINOPHEN, 62207-680 — Acetaminophen, Aspirin and Caffeine, 62207-892 — 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.