Package 72603-129-01

Brand: icosapent ethyl

Generic: icosapent ethyl
NDC Package

Package Facts

Identity

Package NDC 72603-129-01
Digits Only 7260312901
Product NDC 72603-129
Product ID 72603-129_757a9559-dad4-4397-93ac-d81fbaf92754
Description

120 CAPSULE in 1 BOTTLE (72603-129-01)

Marketing

Marketing Status
Marketed Since 2022-01-31
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": "757a9559-dad4-4397-93ac-d81fbaf92754", "openfda": {"upc": ["0372603129014"], "unii": ["6GC8A4PAYH"], "rxcui": ["1304979"], "spl_set_id": ["45f8bb41-bdb1-4afc-83ec-9dc69720ee9c"], "manufacturer_name": ["Northstar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 CAPSULE in 1 BOTTLE (72603-129-01)", "package_ndc": "72603-129-01", "marketing_start_date": "20220131"}], "brand_name": "Icosapent Ethyl", "product_id": "72603-129_757a9559-dad4-4397-93ac-d81fbaf92754", "dosage_form": "CAPSULE", "product_ndc": "72603-129", "generic_name": "Icosapent Ethyl", "labeler_name": "Northstar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Icosapent Ethyl", "active_ingredients": [{"name": "ICOSAPENT ETHYL", "strength": "1 g/1"}], "application_number": "ANDA209457", "marketing_category": "ANDA", "marketing_start_date": "20201104", "listing_expiration_date": "20261231"}