Skip to main content

Oxycodone Hydrochloride

NDC 65162-050 · Amneal Pharmaceuticals LLC

Generic nameOxycodone
Dosage formTABLET
RouteORAL
Active ingredient(s)OXYCODONE HYDROCHLORIDE
Strength20 mg/1
Pharmacologic classFull Opioid Agonists [MoA], Opioid Agonist [EPC]
DEA scheduleCII
Marketing categoryANDA

Packages

65162-050-03 — 30 TABLET in 1 BOTTLE (65162-050-03)

65162-050-10 — 100 TABLET in 1 BOTTLE (65162-050-10)

65162-050-25 — 250 TABLET in 1 BOTTLE (65162-050-25)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

64380-261 — Oxycodone Hydrochloride, 64380-262 — Oxycodone Hydrochloride, 64380-263 — Oxycodone Hydrochloride, 64850-621 — Oxycodone Hydrochloride and Acetaminophen, 64850-622 — Oxycodone Hydrochloride and Acetaminophen, 64850-623 — Oxycodone Hydrochloride and Acetaminophen, 64950-354 — Oxycodone Hydrochloride, 65162-047 — Oxycodone, 65162-048 — Oxycodone, 65162-049 — Oxycodone, 65162-051 — Oxycodone, 65162-207 — Oxycodone and Acetaminophen, 67296-0425 — oxycodone hydrochloride, 67296-0836 — Oxycodone and Acetaminophen, 67296-1937 — Oxycodone and Acetaminophen, 67296-2167 — Oxycodone Hydrochloride, 67296-2188 — Oxycodone Hydrochloride, 67296-2233 — Oxycodone, 68071-2368 — Oxycodone Hydrochloride, 68071-2899 — 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.