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ENDOCET

NDC 72162-1728 · Bryant Ranch Prepack

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

72162-1728-1 — 100 TABLET in 1 BOTTLE (72162-1728-1)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

72162-1334 — Oxycodone Hydrochloride, 72162-1335 — Oxycodone Hydrochloride, 72162-1336 — Oxycodone Hydrochloride, 72162-1337 — Oxycodone Hydrochloride, 72162-1338 — Oxycodone and Acetaminophen, 72162-1339 — Oxycodone and Acetaminophen, 72162-1341 — Hydrocodone Bitartrate and Acetaminophen, 72162-1342 — Hydrocodone Bitartrate and Acetaminophen, 72162-1591 — Butalbital, Acetaminophen, Caffeine and Codeine Phosphate, 72162-1673 — Acetaminophen, 72162-1749 — Oxycodone Hydrochloride, 72162-1811 — Oxycodone, 72162-1812 — Oxycodone, 72162-1989 — Hydrocodone Bitartrate and Acetaminophen, 72162-1990 — Hydrocodone Bitartrate and Acetaminophen, 72162-1991 — Hydrocodone Bitartrate and Acetaminophen, 72162-1996 — hydrocodone bitartrate and acetaminophen, 72162-1997 — hydrocodone bitartrate and acetaminophen, 72162-1998 — hydrocodone bitartrate and acetaminophen, 72162-2001 — acetaminophen and codeine phosphate, +3633 more

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