NDC 10702-023

Oxycodone Hydrochloride 5 mg capsule

On the label: KVK-TECH, Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Kvk-Tech, Inc.Newtown, PA, United StatesMakes it Serious problems, FDA actionMar 14, 2025 · 13 inspections, 3 with FDA action

Product details

Generic drug
Oxycodone: every company that makes it
Form
capsule, oral
Strength
5 mg
Approval
ANDA ANDA202773
On the market since
Aug 20, 2015
Package NDCs
10702-023-01 10702-023-06
Official label
DailyMed (National Library of Medicine), updated Sep 9, 2026

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