NDC 0409-0801
Nipent 2 mg per 1 mL injection, powder, lyophilized, for solution
On the label: Hospira, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Zydus Hospira Oncology Private Limited | Ahmedabad, India | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyJun 30, 2023 · 5 inspections |
Product details
- Generic drug
- Pentostatin: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intravenous
- Strength
- 2 mg per 1 mL
- Approval
- NDA NDA020122
- On the market since
- Aug 15, 2007
- Package NDCs
0409-0801-01- Official label
- DailyMed (National Library of Medicine), updated Oct 19, 2026
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