NDC 68083-707
Epoprostenol 0.5 mg per 10 mL injection, powder, lyophilized, for solution
On the label: Gland Pharma Limited.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Gland Pharma Limited | Hyderabad, India | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyJun 27, 2023 · 4 inspections |
Product details
- Generic drug
- Epoprostenol: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intravenous
- Strength
- 0.5 mg per 10 mL
- Approval
- ANDA ANDA219237
- On the market since
- Dec 29, 2025
- Package NDCs
68083-707-01- Official label
- DailyMed (National Library of Medicine), updated Jan 6, 2026
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