NDC 0143-9606
Azacitidine 100 mg injection, powder, lyophilized, for solution
On the label: Hikma Pharmaceuticals USA Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Thymoorgan GMBH Pharmazie | Goslar OT Vienenburg, Germany | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyMar 26, 2025 · 9 inspections |
Product details
- Generic drug
- Azacitidine: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intravenous; subcutaneous
- Strength
- 100 mg
- Approval
- ANDA ANDA209337
- On the market since
- Jun 8, 2020
- Package NDCs
0143-9606-01- Official label
- DailyMed (National Library of Medicine), updated Apr 11, 2024
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