Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Baxalta Manufacturing Sàrl | Neuchâtel, Switzerland | Makes it and tests it | Not inspected on record |
| Baxalta Us Inc. | Thousand Oaks, CA, United States | Makes the active ingredient, tests it, packages it and labels it | Not inspected on record |
| Baxalta Belgium Manufacturing SA | Lessines, Belgium | Tests it, packages it and labels it | Problems found, fixed voluntarilyJun 18, 2013 · 1 inspection |
| Takeda Manufacturing Austria AG | Orth an der Donau, Austria | Tests it | No problems foundApr 24, 2024 · 1 inspection |
| Takeda Manufacturing Singapore Pte. Ltd. | Singapore, Singapore | Tests it | Not inspected on record |
Product details
- Generic drug
- Antihemophilic Factor, Human Recombinant: every company that makes it
- Form
- kit
- Strength
- 750 [iU] per 2 mL
- Approval
- BLA BLA125566
- On the market since
- Oct 25, 2016
- Package NDCs
0944-4139-010944-4626-010944-4626-020944-4626-0364764-514-02- Official label
- DailyMed (National Library of Medicine), updated May 28, 2026
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