NDC 62756-059
epoprostenol 0.5 mg per 10 mL injection, powder, lyophilized, for solution
On the label: Caraco Pharmaceutical Laboratories, Ltd..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Sun Pharmaceutical Industries, Inc. | Billerica, MA, United States | Makes it and tests it | Problems found, fixed voluntarilyApr 18, 2025 · 15 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 ANDA210473
- On the market since
- Jan 16, 2021
- Package NDCs
62756-059-40- Official label
- DailyMed (National Library of Medicine), updated Apr 23, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?