NDC 0409-0185
Gemcitabine 38 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
- Gemcitabine: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intravenous
- Strength
- 38 mg per 1 mL
- Approval
- ANDA ANDA078339
- On the market since
- Jul 26, 2011
- Package NDCs
0409-0185-01- Official label
- DailyMed (National Library of Medicine), updated Aug 16, 2024
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