NDC 63323-145
Floxuridine 500 mg per 5 mL injection, powder, lyophilized, for solution
On the label: Fresenius Kabi, LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Fresenius Kabi USA, LLC | Melrose Park, IL, United States | Makes it | Problems found, fixed voluntarilyAug 24, 2023 · 13 inspections, 2 with FDA action |
Product details
- Generic drug
- Floxuridine: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intra-arterial
- Strength
- 500 mg per 5 mL
- Approval
- ANDA ANDA075837
- On the market since
- Mar 15, 2001
- Package NDCs
63323-145-07- Official label
- DailyMed (National Library of Medicine), updated Oct 14, 2024
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