Epoprostenol 62756-0060
Product NDC
62756-0060- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Injection, Powder, Lyophilized, For Solution
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- January 16, 2021
- Listing Expires
- December 31, 2026
- Application
- ANDA210473
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Epoprostenol Sodium | 1.5 mg/10mL |
Drug Class
Prostacycline Vasodilator [EPC]Prostaglandins I [CS]Vasodilation [PE]
Packaging Options(1)
1 VIAL in 1 CARTON (62756-060-40) / 10 mL in 1 VIAL