NDC 0409-2337
Deferoxamine Mesylate 2 g 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, intramuscular; intravenous; subcutaneous
- Strength
- 2 g
- Approval
- ANDA ANDA076019
- On the market since
- Mar 31, 2005
- Package NDCs
0409-2337-150409-2337-25- Official label
- DailyMed (National Library of Medicine), updated Apr 6, 2026
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