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Oxycodone Hydrochloride

NDC 13107-057 · Aurolife Pharma, LLC

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

Packages

13107-057-01 — 100 TABLET in 1 BOTTLE (13107-057-01)

13107-057-30 — 30 TABLET in 1 BOTTLE (13107-057-30)

13107-057-99 — 1000 TABLET in 1 BOTTLE (13107-057-99)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

10702-057 — OXYCODONE HYDROCHLORIDE, 10702-171 — oxycodone hydrochloride, 10702-183 — Oxycodone Hydrochloride, 10702-238 — oxycodone and acetaminophen, 13107-043 — Oxycodone and Acetaminophen, 13107-044 — Oxycodone and Acetaminophen, 13107-045 — Oxycodone and Acetaminophen, 13107-046 — Oxycodone and Acetaminophen, 13107-055 — Oxycodone Hydrochloride, 13107-056 — Oxycodone Hydrochloride, 13107-261 — Oxycodone Hydrochloride Oral Solution, 13107-262 — Oxycodone Hydrochloride Oral Solution, 23635-581 — oxycodone hydrochloride, 23635-582 — oxycodone hydrochloride, 31722-191 — Oxycodone and Acetaminophen, 31722-192 — Oxycodone and Acetaminophen, 31722-193 — Oxycodone and Acetaminophen, 31722-194 — Oxycodone and Acetaminophen, 31722-484 — Oxycodone Hydrochloride, 31722-485 — Oxycodone Hydrochloride, +267 more

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