Package 0173-0519-00
Brand: flolan
Generic: epoprostenol sodiumPackage Facts
Identity
Package NDC
0173-0519-00
Digits Only
0173051900
Product NDC
0173-0519
Description
1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 CARTON (0173-0519-00)
Marketing
Marketing Status
Brand
flolan
Generic
epoprostenol sodium
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "38b7a328-0fa3-409f-b230-16bcbc8f4798", "openfda": {"unii": ["4K04IQ1OF4"], "rxcui": ["211199", "211200", "562501", "562502"], "spl_set_id": ["8e4b636e-ee9c-4111-779d-28c8369d283b"], "manufacturer_name": ["GlaxoSmithKline LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 CARTON (0173-0519-00)", "package_ndc": "0173-0519-00", "marketing_end_date": "20260531", "marketing_start_date": "19951208"}], "brand_name": "FLOLAN", "product_id": "0173-0519_38b7a328-0fa3-409f-b230-16bcbc8f4798", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Prostacycline Vasodilator [EPC]", "Prostaglandins I [CS]", "Vasodilation [PE]"], "product_ndc": "0173-0519", "generic_name": "epoprostenol sodium", "labeler_name": "GlaxoSmithKline LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FLOLAN", "active_ingredients": [{"name": "EPOPROSTENOL SODIUM", "strength": "1.5 mg/1"}], "application_number": "NDA020444", "marketing_category": "NDA", "marketing_end_date": "20260531", "marketing_start_date": "19951208"}