Package 67184-0582-1

Brand: icosapent ethyl

Generic: icosapent ethyl
NDC Package

Package Facts

Identity

Package NDC 67184-0582-1
Digits Only 6718405821
Product NDC 67184-0582
Product ID 67184-0582_324fd508-befc-404a-8f75-97b35d2df694
Description

120 CAPSULE in 1 BOTTLE (67184-0582-1)

Marketing

Marketing Status
Marketed Since 2025-01-01
Brand icosapent ethyl
Generic icosapent ethyl
Sample Package No

Linked Drug Pages (1)

Icosapent Ethyl ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "324fd508-befc-404a-8f75-97b35d2df694", "openfda": {"unii": ["6GC8A4PAYH"], "rxcui": ["1304979"], "spl_set_id": ["20686acb-66c5-4d75-9684-7474436e8bef"], "manufacturer_name": ["Qilu Pharmaceutical Co., Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 CAPSULE in 1 BOTTLE (67184-0582-1)", "package_ndc": "67184-0582-1", "marketing_start_date": "20250101"}], "brand_name": "Icosapent Ethyl", "product_id": "67184-0582_324fd508-befc-404a-8f75-97b35d2df694", "dosage_form": "CAPSULE", "product_ndc": "67184-0582", "generic_name": "Icosapent Ethyl", "labeler_name": "Qilu Pharmaceutical Co., Ltd.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Icosapent Ethyl", "active_ingredients": [{"name": "ICOSAPENT ETHYL", "strength": "1 g/1"}], "application_number": "ANDA218899", "marketing_category": "ANDA", "marketing_start_date": "20250101", "listing_expiration_date": "20261231"}