62756-060Level 3
epoprostenol (epoprostenol)
**Product type:** Human Prescription Drug
**Active ingredient:** EPOPROSTENOL SODIUM
**Strength:** 1.5 mg/10mL
**Dosage form:** Injection, Powder, Lyophilized, For Solution
**Route:** Intravenous
**Labeler:** Sun Pharmaceutical Industries, Inc.
**Marketing category:** ANDA (ANDA210473)
**Pharmacologic class:** Prostacycline Vasodilator [EPC], Prostaglandins I [CS], Vasodilation [PE]
GET
/api/v1/systems/ndc_fda/nodes/62756-060Hierarchy Explorer
Loading...
Cross-system equivalences0
No cross-system equivalences mapped for this node.