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Acetaminophen and Codeine Phosphate

NDC 68071-4673 · NuCare 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

68071-4673-2 — 20 TABLET in 1 BOTTLE (68071-4673-2)

68071-4673-3 — 30 TABLET in 1 BOTTLE (68071-4673-3)

68071-4673-4 — 24 TABLET in 1 BOTTLE (68071-4673-4)

68071-4673-5 — 15 TABLET in 1 BOTTLE (68071-4673-5)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68071-3883 — Acetaminophen, 68071-3907 — Acetaminophen, 68071-3914 — Acetaminophen, Aspirin, Caffeine, 68071-3917 — Acetaminophen, 68071-3959 — ACETAMINOPHEN, 68071-4151 — Acetaminophen, 68071-4172 — Acetaminophen, 68071-4475 — acetaminophen and codeine phosphate, 68071-4533 — acetaminophen and codeine phosphate, 68071-4656 — Acetaminophen, 68071-4749 — Acetaminophen and Codeine Phosphate, 68071-4801 — Hydrocodone Bitartrate and Acetaminophen, 68071-4853 — Hydrocodone Bitartrate and Acetaminophen, 68071-4860 — Acetaminophen, 68071-4941 — Hydrocodone Bitartrate and Acetaminophen, 68071-5010 — Acetaminophen and Codeine Phosphate, 68071-5054 — Oxycodone and Acetaminophen, 68071-5169 — Oxycodone and Acetaminophen, 68071-5173 — Codeine Phosphate and Guaifenesin, 68071-5239 — Extra Strength Pain Relief, +3502 more

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