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OXYCODONE AND ACETAMINOPHEN

NDC 72189-255 · DIRECT RX

Generic nameOXYCODONE AND ACETAMINOPHEN
Dosage formTABLET
RouteORAL
Active ingredient(s)OXYCODONE HYDROCHLORIDE, ACETAMINOPHEN
Strength325; 10 mg/1; mg/1
Pharmacologic classFull Opioid Agonists [MoA], Opioid Agonist [EPC]
DEA scheduleCII
Marketing categoryANDA

Packages

72189-255-30 — 30 TABLET in 1 BOTTLE (72189-255-30)

72189-255-60 — 60 TABLET in 1 BOTTLE (72189-255-60)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

72162-2252 — Acetaminophen, 72162-2271 — Hydrocodone Bitartrate and Acetaminophen, 72162-2279 — Acetaminophen, 72162-2404 — Acetaminophen, 72162-2510 — Tramadol Hydrochloride and Acetaminophen, 72162-2665 — BUTALBITAL, ACETAMINOPHEN AND CAFFEINE, 72162-2666 — BUTALBITAL, ACETAMINOPHEN AND CAFFEINE, 72189-094 — OXYCODONE HYDROCHLORIDE, 72189-095 — OXYCODONE HYDROCHLORIDE, 72189-191 — HYDROCODONE BITARTRATE AND ACETAMINOPHEN, 72189-256 — OXYCODONE AND ACETAMINOPHEN, 72189-343 — HYDROCODONE BITARTRATE AND ACETAMINOPHEN, 72189-348 — HYDROCODONE BITARTRATE AND ACETAMINOPHEN, 72189-352 — Hydrocodone APAP, 72189-368 — Oxycodone and Acetaminophen, 72189-375 — Oxycodone/APAP, 72189-376 — Acetaminophen and Codeine Phosphate, 72189-382 — Tramadol Hydrochloride and Acetaminophen, 72189-397 — Oxycodone/APAP, 72189-399 — Hydrocodone/APAP, +3633 more

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