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Acetaminophen and Codeine Phosphate

NDC 68071-3798 · 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

68071-3798-6 — 6 TABLET in 1 BOTTLE (68071-3798-6)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 68071-3658 — acetaminophen and codeine phosphate, 68071-3683 — Oxycodone and Acetaminophen, 68071-3685 — Hydrocodone Bitartrate and Acetaminophen, 68071-3824 — Acetaminophen and Codeine Phosphate, 68071-3869 — Acetaminophen, 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, +3502 more

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