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OxyContin

NDC 59011-410 · Knoa Pharma LLC

Generic nameoxycodone hydrochloride
Dosage formTABLET, FILM COATED, EXTENDED RELEASE
RouteORAL
Active ingredient(s)OXYCODONE HYDROCHLORIDE
Strength10 mg/1
Pharmacologic classFull Opioid Agonists [MoA], Opioid Agonist [EPC]
DEA scheduleCII
Marketing categoryNDA

Packages

59011-410-10 — 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59011-410-10)

59011-410-20 — 2 BLISTER PACK in 1 CARTON (59011-410-20) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

47781-264 — Oxycodone hydrochloride, 47781-265 — Oxycodone hydrochloride, 49999-852 — Oxycodone and Acetaminophen, 49999-899 — Oxycodone Hydchloride, 50268-644 — Oxycodone and Acetaminophen, 50268-645 — Oxycodone and Acetaminophen, 50268-646 — Oxycodone and Acetaminophen, 53746-203 — Oxycodone and Acetaminophen, 53746-204 — Oxycodone and Acetaminophen, 55700-174 — OXYCODONE HYDROCHLORIDE, 59011-415 — oxycodone hydrochloride, 59011-420 — oxycodone hydrochloride, 59011-430 — oxycodone hydrochloride, 59011-440 — oxycodone hydrochloride, 59011-460 — oxycodone hydrochloride, 59011-480 — oxycodone hydrochloride, 60687-406 — Oxycodone Hydrochloride, 60687-642 — Oxycodone and Acetaminophen, 60760-897 — Oxycodone and Acetaminophen, 60760-898 — Oxycodone and Acetaminophen, +267 more

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

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels