NDC 72189-094
Oxycodone Hydrochloride 10 mg tablet
On the label: Direct Rx. It's repackaged: Direct Rx rebottles it from KVK-TECH, Inc.'s NDC 10702-056.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Kvk-Tech, Inc. | Newtown, PA, United States | Makes it | Serious problems, FDA actionMar 14, 2025 · 13 inspections, 3 with FDA action |
Repackaging site
- Direct Rx, Dawsonville, GA, United States · repackages it
Product details
- Generic drug
- Oxycodone: every company that makes it
- Form
- tablet, oral
- Strength
- 10 mg
- Approval
- ANDA ANDA091393
- On the market since
- Jun 15, 2020
- Package NDCs
72189-094-3072189-094-6072189-094-90- Official label
- DailyMed (National Library of Medicine), updated Jun 5, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?