NDC 63323-771
Azacitidine 100 mg per 30 mL injection, powder, lyophilized, for solution
On the label: Fresenius Kabi, LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Shilpa Medicare Limited | Mahabubnagar, India | Makes it, tests it and packages it | Serious problems, FDA actionFeb 25, 2020 · 6 inspections, 1 with FDA action |
Product details
- Generic drug
- Azacitidine: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intravenous; subcutaneous
- Strength
- 100 mg per 30 mL
- Approval
- ANDA ANDA207518
- On the market since
- Mar 16, 2017
- Package NDCs
63323-771-39- Official label
- DailyMed (National Library of Medicine), updated Jun 18, 2025
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