Package 0173-0517-00

Brand: FLOLAN

Generic: epoprostenol sodium
NDC Package

Package Facts

Identity

Package NDC 0173-0517-00
Digits Only 0173051700
Product NDC 0173-0517
Description

1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 CARTON (0173-0517-00)

Marketing

Marketing Status
Marketed Since 1995-12-08
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": "5e54002e-7b03-46ad-ae01-c76c76967201", "openfda": {"unii": ["059QF0KO0R", "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 (0173-0517-00)", "package_ndc": "0173-0517-00", "marketing_start_date": "19951208"}], "brand_name": "FLOLAN", "product_id": "0173-0517_5e54002e-7b03-46ad-ae01-c76c76967201", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Prostacycline Vasodilator [EPC]", "Prostaglandins I [CS]", "Vasodilation [PE]"], "product_ndc": "0173-0517", "generic_name": "epoprostenol sodium", "labeler_name": "GlaxoSmithKline LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FLOLAN", "active_ingredients": [{"name": "EPOPROSTENOL SODIUM", "strength": ".5 mg/1"}], "application_number": "NDA020444", "marketing_category": "NDA", "marketing_start_date": "19951208", "listing_expiration_date": "20261231"}