NDC 79672-825
Oxaliplatin 50 mg per 10 mL injection, powder, lyophilized, for solution
On the label: Nextgen Pharmaceuticals LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Qilu Pharmaceutical (Hainan) Co., Ltd. | Haikou, China | Makes 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
- Strength
- 50 mg per 10 mL
- Approval
- ANDA ANDA204616
- On the market since
- Jul 1, 2020
- Package NDCs
79672-825-02- Official label
- DailyMed (National Library of Medicine), updated Dec 26, 2023
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?