Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Excella GmbH & Co. KG | Feucht, Germany | Makes the active ingredient and tests it | Problems found, fixed voluntarilyOct 19, 2022 · 7 inspections |
| Novartis Pharma Stein AG | Stein, Switzerland | Makes it, tests it and packages it | Problems found, fixed voluntarilyJul 19, 2024 · 9 inspections |
| Wasserburger Arzneimittelwerk GmbH | Wasserburg a Inn, Germany | Makes it, tests it and packages it | No problems foundMay 2, 2024 · 5 inspections |
| Labor LS SE & Co. KG | Bad Bocklet, Germany | Tests it | Problems found, fixed voluntarilyDec 14, 2022 · 6 inspections, 1 with FDA action |
| Novartis Pharma AG | Basel, Switzerland | Tests it | Problems found, fixed voluntarilyDec 18, 2025 · 10 inspections |
| Packaging Coordinators, LLC | Philadelphia, PA, United States | Packages it | Problems found, fixed voluntarilyJan 31, 2025 · 6 inspections |
| Pharmanalytica SA | Locarno, Switzerland | Tests it | No problems foundMar 29, 2023 · 4 inspections |
| SGS Institut Fresenius GmbH | Berlin, Germany | Tests it | No problems foundNov 23, 2023 · 6 inspections |
| SGS Institut Fresenius GmbH | Taunusstein, Germany | Tests it | Problems found, fixed voluntarilyFeb 21, 2025 · 4 inspections |
| SGS International Services Laboratory (ISL) Limited | Cork, Ireland | Tests it | No problems foundApr 14, 2022 · 3 inspections |
| Solvias AG | Kaiseraugst, Switzerland | Tests it | Problems found, fixed voluntarilyAug 7, 2025 · 10 inspections |
Product details
- Generic drug
- Deferoxamine: every company that makes it
- Form
- injection, powder, for solution, intravenous; subcutaneous
- Strength
- 500 mg per 5 mL
- Approval
- NDA NDA016267
- On the market since
- Apr 2, 1968
- Package NDCs
87081-467-91- Official label
- DailyMed (National Library of Medicine), updated Jul 2, 2025
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