NDC 67184-0502
Oxaliplatin 100 mg per 20 mL injection, powder, lyophilized, for solution
On the label: Qilu Pharmaceutical Co., Ltd..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Qilu Pharmaceutical (Hainan) Co., Ltd. | Haikou, China | Makes it and tests it | Problems found, fixed voluntarilyMay 19, 2023 · 5 inspections |
Product details
- Generic drug
- Oxaliplatin: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intravenous
- Strength
- 100 mg per 20 mL
- Approval
- ANDA ANDA204616
- On the market since
- May 11, 2016
- Package NDCs
67184-0502-1- Official label
- DailyMed (National Library of Medicine), updated Oct 18, 2021
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