NDC 60760-957

Oxycodone Hydrochloride 15 mg tablet

On the label: St. Mary's Medical Park Pharmacy. It's repackaged: St. Mary's Medical Park Pharmacy rebottles it from KVK-TECH, Inc.'s NDC 10702-008.

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
15 mg
Approval
ANDA ANDA091393
On the market since
Oct 18, 2013
Package NDCs
60760-957-30 60760-957-60 60760-957-90
Official label
DailyMed (National Library of Medicine), updated May 19, 2026

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