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Percocet

NDC 72189-397 · Direct_Rx

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

Packages

72189-397-30 — 30 TABLET in 1 BOTTLE (72189-397-30)

72189-397-60 — 60 TABLET in 1 BOTTLE (72189-397-60)

72189-397-72 — 120 TABLET in 1 BOTTLE (72189-397-72)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

72189-191 — HYDROCODONE BITARTRATE AND ACETAMINOPHEN, 72189-255 — OXYCODONE 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, 72189-399 — Hydrocodone/APAP, 72189-406 — HYDROCODONE/APAP, 72189-407 — Hydrocodone/APAP, 72189-441 — Butal/APAP/Caff, 72189-600 — BUTAL/APAP/CAFFEINE, 72189-611 — Oxycodone HCL, 72189-613 — Oxycodone HCL, 72189-614 — Oxycodone HCL, 72189-618 — Oxycodone HCL, 72189-632 — Oxycodone HCL, +3633 more

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