NDC 81643-9270
Floxuridine 500 mg injection, powder, lyophilized, for solution
On the label: JND Therapeutics, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Thymoorgan GMBH Pharmazie | Goslar OT Vienenburg, Germany | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyMar 26, 2025 · 9 inspections |
Product details
- Generic drug
- Floxuridine: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intra-arterial
- Strength
- 500 mg
- Approval
- ANDA ANDA075387
- On the market since
- Jun 9, 2022
- Package NDCs
81643-9270-1- Official label
- DailyMed (National Library of Medicine), updated Oct 7, 2024
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