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Oxycodone Hydrochloride

NDC 31722-485 · Camber Pharmaceuticals Inc

Generic nameOxycodone Hydrochloride
Dosage formTABLET
RouteORAL
Active ingredient(s)OXYCODONE HYDROCHLORIDE
Strength10 mg/1
Pharmacologic classFull Opioid Agonists [MoA], Opioid Agonist [EPC]
DEA scheduleCII
Marketing categoryANDA

Packages

31722-485-01 — 100 TABLET in 1 BOTTLE (31722-485-01)

31722-485-05 — 500 TABLET in 1 BOTTLE (31722-485-05)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

13107-057 — 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, 31722-486 — Oxycodone Hydrochloride, 31722-917 — Oxycodone Hydrochloride, 31722-918 — Oxycodone Hydrochloride, 31722-948 — Oxycodone and Acetaminophen, 31722-949 — Oxycodone and Acetaminophen, 31722-950 — Oxycodone and Acetaminophen, 31722-951 — Oxycodone and Acetaminophen, 35356-839 — Oxycodone Hydchloride, 40032-950 — Oxycodone Hydrochloride, 42806-005 — 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.