NDC 82511-008
Gemcitabine hydrochloride 200 mg per 5 mL injection, powder, lyophilized, for solution
On the label: Teyro Labs Private Limited.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Teyro Labs Private Limited | Kanchipuram District, India | Makes it, tests it and packages it | Problems found, fixed voluntarilyNov 12, 2025 · 1 inspection |
Product details
- Generic drug
- Gemcitabine: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intravenous
- Strength
- 200 mg per 5 mL
- Approval
- ANDA ANDA078759
- On the market since
- Aug 8, 2024
- Package NDCs
82511-008-20- Official label
- DailyMed (National Library of Medicine), updated Jan 9, 2025
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