NDC 13107-261
Oxycodone Hydrochloride Oral Solution 5 mg per 5 mL solution
On the label: Aurolife Pharma LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurolife Pharma LLC | Dayton, NJ, United States | Makes it, tests it, packages it and labels it | Serious problems, FDA actionDec 7, 2021 · 10 inspections, 1 with FDA action |
Product details
- Generic drug
- Oxycodone: every company that makes it
- Form
- solution, oral
- Strength
- 5 mg per 5 mL
- Approval
- ANDA ANDA212429
- On the market since
- Jan 27, 2020
- Package NDCs
13107-261-58- Official label
- DailyMed (National Library of Medicine), updated Jan 18, 2024
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