NDC 47335-178
Oxaliplatin 100 mg per 20 mL injection, powder, lyophilized, for solution
On the label: Caraco Pharmaceutical Laboratories, Ltd..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Sun Pharmaceutical Industries Limited | Halol, India | Makes it and tests it | Serious problems, FDA actionJun 13, 2025 · 12 inspections, 5 with FDA action |
Product details
- Generic drug
- Oxaliplatin: every company that makes it
- Form
- injection, powder, lyophilized, for solution
- Strength
- 100 mg per 20 mL
- Approval
- ANDA ANDA078818
- On the market since
- Aug 19, 2009
- Package NDCs
47335-178-40- Official label
- DailyMed (National Library of Medicine), updated Oct 25, 2018
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