NDC 55700-175
Oxycodone Hydrochloride 30 mg tablet
On the label: Lake Erie Medical DBA Quality Care Products LLC. It's repackaged: Lake Erie Medical DBA Quality Care Products LLC rebottles it from KVK-TECH, Inc.'s NDC 10702-009.
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
- Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC, Location not on file · repackages it
Product details
- Generic drug
- Oxycodone: every company that makes it
- Form
- tablet
- Strength
- 30 mg
- Approval
- ANDA ANDA091393
- On the market since
- Oct 18, 2013
- Package NDCs
55700-175-0155700-175-3055700-175-6055700-175-90- Official label
- DailyMed (National Library of Medicine), updated Dec 19, 2024
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