NDC 68001-642
Decitabine 50 mg per 10 mL injection, powder, lyophilized, for solution
On the label: BluePoint Laboratories..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Hetero Labs Limited | Mahabubnagar, India | Makes it | Problems found, fixed voluntarilyJun 26, 2026 · 4 inspections, 1 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 ANDA215355
- On the market since
- May 1, 2025
- Package NDCs
68001-642-41- Official label
- DailyMed (National Library of Medicine), updated Sep 29, 2025
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