NDC 70121-1644
Decitabine 50 mg per 20 mL injection, powder, lyophilized, for solution
On the label: Amneal Pharmaceuticals LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Kelix bio (Malta) Ltd. | Birzebbugia, Malta | Makes it | Problems found, fixed voluntarilyDec 16, 2022 · 1 inspection |
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 ANDA206033
- On the market since
- Dec 1, 2019
- Package NDCs
70121-1644-1- Official label
- DailyMed (National Library of Medicine), updated Feb 12, 2021
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