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Oxycodone Hydrochloride

NDC 72162-1812 · Bryant Ranch Prepack

Generic nameOxycodone
Dosage formTABLET
RouteORAL
Active ingredient(s)OXYCODONE HYDROCHLORIDE
Strength30 mg/1
Pharmacologic classFull Opioid Agonists [MoA], Opioid Agonist [EPC]
DEA scheduleCII
Marketing categoryANDA

Packages

72162-1812-0 — 60 TABLET in 1 BOTTLE (72162-1812-0)

72162-1812-1 — 90 TABLET in 1 BOTTLE (72162-1812-1)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71930-047 — oxycodone and acetaminophen, 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, 72162-1728 — Oxycodone and Acetaminophen, 72162-1749 — Oxycodone Hydrochloride, 72162-1811 — Oxycodone, 72189-094 — OXYCODONE HYDROCHLORIDE, 72189-095 — OXYCODONE HYDROCHLORIDE, 72189-255 — OXYCODONE AND ACETAMINOPHEN, 72189-256 — OXYCODONE AND ACETAMINOPHEN, 72189-368 — Oxycodone and Acetaminophen, 72189-375 — Oxycodone/APAP, 72189-397 — Oxycodone/APAP, 72189-611 — Oxycodone HCL, 72189-613 — Oxycodone HCL, 72189-614 — Oxycodone HCL, +267 more

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