NDC 71335-1361
Oxycodone Hydrochloride 5 mg tablet
On the label: Bryant Ranch Prepack. It's repackaged: Bryant Ranch Prepack rebottles it from Aurolife Pharma LLC's NDC 13107-055.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurolife Pharma LLC | Dayton, NJ, United States | Makes it | Serious problems, FDA actionDec 7, 2021 · 10 inspections, 1 with FDA action |
Repackaging site
- Bryant Ranch Prepack, Burbank, CA, United States · repackages it and relabels it
Product details
- Generic drug
- Oxycodone: every company that makes it
- Form
- tablet, oral
- Strength
- 5 mg
- Approval
- ANDA ANDA202160
- On the market since
- Jul 12, 2012
- Package NDCs
71335-1361-071335-1361-171335-1361-271335-1361-371335-1361-471335-1361-571335-1361-671335-1361-771335-1361-871335-1361-9- Official label
- DailyMed (National Library of Medicine), updated Aug 12, 2024
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