NDC 61703-363
Oxaliplatin 5 mg per 1 mL injection, solution, concentrate
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
- Oxaliplatin: every company that makes it
- Form
- injection, solution, concentrate, intravenous
- Strength
- 5 mg per 1 mL
- Approval
- ANDA ANDA078813
- On the market since
- Aug 10, 2009
- Package NDCs
61703-363-1861703-363-22- Official label
- DailyMed (National Library of Medicine), updated Aug 7, 2026
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