Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Zydus Lifesciences Limited | Ahmedabad, India | Makes it and tests it | Problems found, fixed voluntarilyJun 17, 2025 · 9 inspections, 1 with FDA action |
Product details
- Generic drug
- Nelarabine: every company that makes it
- Form
- injection, intravenous
- Strength
- 5 mg per 1 mL
- Approval
- ANDA ANDA215037
- On the market since
- Nov 17, 2021
- Package NDCs
70771-1685-170771-1685-8- Official label
- DailyMed (National Library of Medicine), updated Nov 5, 2022
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