Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Dr.reddy's Laboratories Limited | Visakhapatnam, India | Makes it and tests it | Problems found, fixed voluntarilyMay 17, 2024 · 9 inspections, 2 with FDA action |
Product details
- Generic drug
- Nelarabine: every company that makes it
- Form
- injection, intravenous
- Strength
- 5 mg per 1 mL
- Approval
- ANDA ANDA216934
- On the market since
- Jan 9, 2023
- Package NDCs
43598-142-0643598-142-11- Official label
- DailyMed (National Library of Medicine), updated Mar 29, 2025
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