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OXYCODONE HYDROCHLORIDE

NDC 0115-1560 · Amneal Pharmaceuticals of New York LLC

Generic nameOXYCODONE HYDROCHLORIDE
Dosage formTABLET, FILM COATED, EXTENDED RELEASE
RouteORAL
Active ingredient(s)OXYCODONE HYDROCHLORIDE
Strength40 mg/1
Pharmacologic classFull Opioid Agonists [MoA], Opioid Agonist [EPC]
DEA scheduleCII
Marketing categoryNDA AUTHORIZED GENERIC

Packages

0115-1560-01 — 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0115-1560-01)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0054-0390 — oxycodone hydrochloride, 0121-0827 — OXYCODONE HYDROCHLORIDE, 0121-4827 — OXYCODONE HYDROCHLORIDE, 0406-0512 — oxycodone hydrochloride and acetaminophen, 0406-0522 — oxycodone hydrochloride and acetaminophen, 0406-0523 — oxycodone hydrochloride and acetaminophen, 0406-0552 — oxycodone hydrochloride, 0406-8510 — oxycodone hydrochloride, 0406-8515 — oxycodone hydrochloride, 0406-8520 — oxycodone hydrochloride, 0406-8530 — oxycodone hydrochloride, 0406-8556 — Oxycodone Hydrochloride, 0406-8557 — Oxycodone Hydrochloride, 0904-6678 — Oxycodone Hydrochloride, 0904-6828 — Oxycodone Hydrochloride, 0904-6966 — Oxycodone, 0904-7093 — oxycodone and acetaminophen, 0904-7094 — oxycodone and acetaminophen, 0904-7095 — oxycodone and acetaminophen, 0904-7180 — Oxycodone, +267 more

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