NDC 65219-380
Allopurinol 500 mg per 25 mL injection, powder, lyophilized, for solution
On the label: Fresenius Kabi USA, LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Gland Pharma Limited | Hyderabad, India | Makes it, tests it and packages it | Problems found, fixed voluntarilyJul 25, 2024 · 7 inspections |
Product details
- Generic drug
- Allopurinol: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intravenous
- Strength
- 500 mg per 25 mL
- Approval
- ANDA ANDA212363
- On the market since
- Mar 14, 2022
- Package NDCs
65219-380-30- Official label
- DailyMed (National Library of Medicine), updated Jan 24, 2023
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