FDA
Epoprostenol Sodium
The FDA lists this product in 8 strengths and forms.
Composition
- Active ingredients
- EPOPROSTENOL SODIUM EQ 0.5MG BASE/VIAL
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- EPOPROSTENOL SODIUM EQ 0.5MG BASE/VIAL · InjectableThis page
- EPOPROSTENOL SODIUM EQ 1.5MG BASE/VIAL · InjectableANDA078396-002 · Prescription
- EPOPROSTENOL SODIUM EQ 0.5MG BASE/VIAL · InjectableANDA210473-001 · Prescription
- EPOPROSTENOL SODIUM EQ 1.5MG BASE/VIAL · InjectableANDA210473-002 · Prescription
- EPOPROSTENOL SODIUM EQ 1.5MG BASE/VIAL · InjectableANDA213913-002 · Prescription
- EPOPROSTENOL SODIUM EQ 0.5MG BASE/VIAL · InjectableANDA213913-001 · Prescription
- EPOPROSTENOL SODIUM EQ 1.5MG BASE/VIAL · InjectableANDA219237-002 · Prescription
- EPOPROSTENOL SODIUM EQ 0.5MG BASE/VIAL · InjectableANDA219237-001 · Prescription
Official product information
Drugs@FDA lists the approved labels, letters and reviews for application ANDA078396.
At a glance
- Brand name
- Epoprostenol Sodium
- Route
- Injection
- Dosage form
- Injectable
- Applicant
- Meitheal
- Status
- Prescription
- FDA approval
- 23 Apr 2008
- Application
- ANDA078396-001