| NDC Code | 62756-060-40 |
|---|
| Package Description | 1 VIAL in 1 CARTON (62756-060-40) / 10 mL in 1 VIAL |
|---|
| Product NDC | 62756-060 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Epoprostenol |
|---|
| Non-Proprietary Name | Epoprostenol |
|---|
| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
|---|
| Usage | INTRAVENOUS |
|---|
| Start Marketing Date | 20210116 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA210473 |
|---|
| Manufacturer | Sun Pharmaceutical Industries, Inc. |
|---|
| Substance Name | EPOPROSTENOL SODIUM |
|---|
| Strength | 1.5 |
|---|
| Strength Unit | mg/10mL |
|---|
| Pharmacy Classes | Prostacycline Vasodilator [EPC], Prostaglandins I [CS], Vasodilation [PE] |
|---|