NDC 61703-349
Irinotecan Hydrochloride 20 mg per 1 mL injection, solution
On the label: Hospira, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Zydus Hospira Oncology Private Limited | Ahmedabad, India | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyJun 30, 2023 · 5 inspections |
Product details
- Generic drug
- Irinotecan: every company that makes it
- Form
- injection, solution, intravenous
- Strength
- 20 mg per 1 mL
- Approval
- ANDA ANDA077915
- On the market since
- Feb 27, 2008
- Package NDCs
61703-349-0961703-349-1661703-349-36- Official label
- DailyMed (National Library of Medicine), updated Nov 3, 2025
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