NDC 68001-618
Decitabine 50 mg per 20 mL injection, powder, lyophilized, for solution
On the label: BluePoint Laboratories..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Qilu Pharmaceutical (Hainan) Co., Ltd. | Haikou, China | Makes it, tests it and packages it | Problems found, fixed voluntarilyMay 19, 2023 · 5 inspections |
Product details
- Generic drug
- Decitabine: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intravenous
- Strength
- 50 mg per 20 mL
- Approval
- ANDA ANDA212826
- On the market since
- May 3, 2024
- Package NDCs
68001-618-37- Official label
- DailyMed (National Library of Medicine), updated Aug 5, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?