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Oxycodone and Acetaminophen

NDC 68071-5169 · NuCare Pharmaceuticals,Inc.

Generic nameOxycodone and Acetaminophen
Dosage formTABLET
RouteORAL
Active ingredient(s)OXYCODONE HYDROCHLORIDE, ACETAMINOPHEN
Strength325; 5 mg/1; mg/1
Pharmacologic classFull Opioid Agonists [MoA], Opioid Agonist [EPC]
DEA scheduleCII
Marketing categoryANDA

Packages

68071-5169-2 — 20 TABLET in 1 BOTTLE (68071-5169-2)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68071-4533 — acetaminophen and codeine phosphate, 68071-4656 — Acetaminophen, 68071-4673 — Acetaminophen and Codeine Phosphate, 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, 68071-5239 — Extra Strength Pain Relief, 68071-5300 — ACETAMINOPHEN, 68083-647 — Acetaminophen, 68083-648 — Acetaminophen, 68084-354 — OXYCODONE HYDROCHLORIDE, 68084-699 — Oxycodone and Acetaminophen, 68084-710 — Oxycodone and Acetaminophen, 68084-968 — OXYCODONE HYDROCHLORIDE, 68084-975 — OXYCODONE HYDROCHLORIDE, 68084-983 — OXYCODONE HYDROCHLORIDE, +3633 more

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