NDC 62756-059

epoprostenol

Epoprostenol

epoprostenol is a Intravenous Injection, Powder, Lyophilized, For Solution in the Human Prescription Drug category. It is labeled and distributed by Sun Pharmaceutical Industries, Inc.. The primary component is Epoprostenol Sodium.

• Product ID: 62756-059_4a908d55-af35-4d85-b188-37a7ffad2e71
• NDC: 62756-059
• Product Type: Human Prescription Drug
• Proprietary Name: epoprostenol
• Generic Name: Epoprostenol
• Dosage Form: Injection, Powder, Lyophilized, For Solution
• Route of Administration: INTRAVENOUS
• Marketing Start Date: 2021-01-16
• Marketing Category: ANDA / ANDA
• Application Number: ANDA210473
• Labeler Name: Sun Pharmaceutical Industries, Inc.
• Substance Name: EPOPROSTENOL SODIUM
• Active Ingredient Strength: 1 mg/10mL
• Pharm Classes: Prostacycline Vasodilator [EPC],Prostaglandins I [CS],Vasodilation [PE]
• NDC Exclude Flag: N
• Listing Certified Through: 2022-12-31

Packaging

NDC 62756-059-40

1 VIAL in 1 CARTON (62756-059-40) > 10 mL in 1 VIAL

• Marketing Start Date: 2021-01-16
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 62756-059-40 [62756005940]

epoprostenol INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

• Marketing Category: ANDA
• Application Number: ANDA210473
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2018-04-30
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
EPOPROSTENOL SODIUM	.5 mg/10mL

Pharmacological Class

• Prostacycline Vasodilator [EPC]
• Prostaglandins I [CS]
• Vasodilation [PE]

NDC Crossover Matching brand name "epoprostenol" or generic name "Epoprostenol"

NDC	Brand Name	Generic Name
62756-059	epoprostenol	epoprostenol
62756-060	epoprostenol	epoprostenol
66215-402	Veletri	epoprostenol
66215-403	Veletri	epoprostenol