NDC 68083-172
Deferoxamine mesylate 500 mg injection, powder, lyophilized, for solution
On the label: Gland Pharma Limited.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Gland Pharma Limited | Hyderabad, India | Makes it, tests it, packages it and labels 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, intramuscular; intravenous; subcutaneous
- Strength
- 500 mg
- Approval
- ANDA ANDA207384
- On the market since
- Oct 9, 2017
- Package NDCs
68083-172-01- Official label
- DailyMed (National Library of Medicine), updated Mar 6, 2026
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