NDC 31722-486

Oxycodone Hydrochloride 20 mg tablet

On the label: Camber Pharmaceuticals Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Ascent Pharmaceuticals IncCentral Islip, NY, United StatesMakes it, tests it and packages it Problems found, fixed voluntarilyAug 9, 2024 · 9 inspections

Recalls

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Product details

Generic drug
Oxycodone: every company that makes it
Form
tablet, oral
Strength
20 mg
Approval
ANDA ANDA207418
On the market since
Nov 14, 2025
Package NDCs
31722-486-01 31722-486-05
Official label
DailyMed (National Library of Medicine), updated Jan 14, 2026

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