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Oxycodone Hydrochloride

NDC 43386-431 · Lupin Pharmaceuticals,Inc.

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

43386-431-01 — 100 TABLET in 1 BOTTLE (43386-431-01)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

42806-116 — Oxycodone and Acetaminophen, 42858-001 — Oxycodone Hydrochloride, 42858-002 — Oxycodone Hydrochloride, 42858-003 — Oxycodone Hydrochloride, 42858-004 — Oxycodone Hydrochloride, 42858-005 — Oxycodone Hydrochloride, 42858-102 — Oxycodone and Acetaminophen, 42858-103 — Oxycodone and Acetaminophen, 42858-104 — Oxycodone and Acetaminophen, 43386-430 — Oxycodone Hydrochloride, 43386-432 — Oxycodone Hydrochloride, 43386-433 — Oxycodone Hydrochloride, 43386-434 — Oxycodone Hydrochloride, 43386-490 — Oxycodone and Acetaminophen, 43386-491 — Oxycodone and Acetaminophen, 43386-492 — Oxycodone and Acetaminophen, 43386-493 — Oxycodone and Acetaminophen, 43386-920 — Oxycodone Hydrochloride, 43602-190 — OXYCODONE HYDROCHLORIDE, 43602-198 — 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.