NDC 0409-2336
Deferoxamine Mesylate 500 mg injection, powder, lyophilized, for solution
On the label: Hospira, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Hospira, Inc. | McPherson, KS, United States | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyJan 17, 2025 · 16 inspections, 2 with FDA action |
Product details
- Generic drug
- Deferoxamine: every company that makes it
- Form
- injection, powder, lyophilized, for solution
- Strength
- 500 mg
- Approval
- ANDA ANDA076019
- On the market since
- Apr 30, 2005
- Package NDCs
0409-2336-010409-2336-10- Official label
- DailyMed (National Library of Medicine), updated Apr 6, 2026
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