NDC 71335-1245

Oxycodone Hydrochloride 30 mg tablet

On the label: Bryant Ranch Prepack. It's repackaged: Bryant Ranch Prepack rebottles it from KVK-TECH, Inc.'s NDC 10702-009.

United States: 1

Where the pills inside were made

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

Repackaging site

Product details

Generic drug
Oxycodone: every company that makes it
Form
tablet, oral
Strength
30 mg
Approval
ANDA ANDA091393
On the market since
Oct 18, 2013
Package NDCs
71335-1245-1 71335-1245-2 71335-1245-3 71335-1245-4 71335-1245-5 71335-1245-6 71335-1245-7 71335-1245-8
Official label
DailyMed (National Library of Medicine), updated Jul 14, 2026

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