Package 62756-060-40
Brand: epoprostenol
Generic: epoprostenolPackage Facts
Identity
Package NDC
62756-060-40
Digits Only
6275606040
Product NDC
62756-060
Description
1 VIAL in 1 CARTON (62756-060-40) / 10 mL in 1 VIAL
Marketing
Marketing Status
Brand
epoprostenol
Generic
epoprostenol
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "fae129b5-c1b5-45f2-864c-eee72f289334", "openfda": {"upc": ["0362756059405", "0362756060401"], "unii": ["4K04IQ1OF4"], "rxcui": ["562501", "562502"], "spl_set_id": ["db57e498-db20-45e8-8298-b0cf0811d270"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (62756-060-40) / 10 mL in 1 VIAL", "package_ndc": "62756-060-40", "marketing_start_date": "20210116"}], "brand_name": "epoprostenol", "product_id": "62756-060_fae129b5-c1b5-45f2-864c-eee72f289334", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Prostacycline Vasodilator [EPC]", "Prostaglandins I [CS]", "Vasodilation [PE]"], "product_ndc": "62756-060", "generic_name": "epoprostenol", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "epoprostenol", "active_ingredients": [{"name": "EPOPROSTENOL SODIUM", "strength": "1.5 mg/10mL"}], "application_number": "ANDA210473", "marketing_category": "ANDA", "marketing_start_date": "20210116", "listing_expiration_date": "20261231"}