NDC 13107-055

Oxycodone Hydrochloride 5 mg tablet

On the label: Aurolife Pharma LLC.

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Aurolife Pharma LLCDayton, NJ, United StatesMakes it Serious problems, FDA actionDec 7, 2021 · 10 inspections, 1 with FDA action

Product details

Generic drug
Oxycodone: every company that makes it
Form
tablet, oral
Strength
5 mg
Approval
ANDA ANDA202160
On the market since
Jul 12, 2012
Package NDCs
13107-055-01 13107-055-30 13107-055-99
Official label
DailyMed (National Library of Medicine), updated Dec 23, 2025

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