NDC 43598-427
Decitabine 50 mg per 10 mL injection, powder, lyophilized, for solution
On the label: Dr. Reddy's Laboratories Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Dr.reddy's Laboratories Limited | Visakhapatnam, India | Makes it and tests it | Problems found, fixed voluntarilyMay 17, 2024 · 9 inspections, 2 with FDA action |
Product details
- Generic drug
- Decitabine: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intravenous
- Strength
- 50 mg per 10 mL
- Approval
- ANDA ANDA203131
- On the market since
- Dec 5, 2014
- Package NDCs
43598-427-37- Official label
- DailyMed (National Library of Medicine), updated Mar 25, 2026
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