NDC 68001-620
Azacitidine 100 mg injection, powder, lyophilized, for solution
On the label: BluePoint Laboratories..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| DR Reddy's Laboratories Limited | Srikakulam, India | Makes it and tests it | Problems found, fixed voluntarilyJul 18, 2025 · 1 inspection |
Product details
- Generic drug
- Azacitidine: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intravenous; subcutaneous
- Strength
- 100 mg
- Approval
- ANDA ANDA201537
- On the market since
- Jan 10, 2025
- Package NDCs
68001-620-54- Official label
- DailyMed (National Library of Medicine), updated Mar 26, 2026
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