NDC 52609-4505
Deferoxamine mesylate 500 mg injection, powder, lyophilized, for solution
On the label: ApoPharma USA, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Gland Pharma Limited | Hyderabad, India | Makes it, makes the active ingredient, tests it and packages it | Problems found, fixed voluntarilyJul 25, 2024 · 7 inspections |
Product details
- Generic drug
- Deferoxamine: every company that makes it
- Form
- injection, powder, lyophilized, for solution
- Strength
- 500 mg
- Approval
- ANDA ANDA207384
- On the market since
- Mar 23, 2018
- Package NDCs
52609-4505-6- Official label
- DailyMed (National Library of Medicine), updated Mar 23, 2018
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