NDC 68001-442
Cyclophosphamide 500 mg per 25 mL injection, powder, for solution
On the label: BluePoint Laboratories..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Simtra Deutschland GmbH | Halle/Westfalen, Germany | Makes it, tests it, packages it, labels it and sterilizes it | Serious problems, FDA actionSep 26, 2025 · 11 inspections, 1 with FDA action |
Product details
- Generic drug
- 4-Hydroxycyclophosphamide: every company that makes it
- Form
- injection, powder, for solution, intravenous; oral
- Strength
- 500 mg per 25 mL
- Approval
- ANDA ANDA040745
- On the market since
- Oct 19, 2020
- Package NDCs
68001-442-26- Official label
- DailyMed (National Library of Medicine), updated Feb 12, 2026
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