Package 0054-0621-27

Brand: icosapent ethyl

Generic: icosapent ethyl
NDC Package

Package Facts

Identity

Package NDC 0054-0621-27
Digits Only 0054062127
Product NDC 0054-0621
Description

240 CAPSULE in 1 BOTTLE (0054-0621-27)

Marketing

Marketing Status
Marketed Since 2023-03-09
Brand icosapent ethyl
Generic icosapent ethyl
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2417e4be-d579-4c3d-8ec0-a42dc51aabf5", "openfda": {"upc": ["0300540621278", "0300540508234"], "unii": ["6GC8A4PAYH"], "rxcui": ["1304979", "1811180"], "spl_set_id": ["e3d38d1d-fbe7-413d-849a-675e7dfa9b0a"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "240 CAPSULE in 1 BOTTLE (0054-0621-27)", "package_ndc": "0054-0621-27", "marketing_start_date": "20230309"}], "brand_name": "Icosapent Ethyl", "product_id": "0054-0621_2417e4be-d579-4c3d-8ec0-a42dc51aabf5", "dosage_form": "CAPSULE", "product_ndc": "0054-0621", "generic_name": "Icosapent Ethyl", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Icosapent Ethyl", "active_ingredients": [{"name": "ICOSAPENT ETHYL", "strength": ".5 g/1"}], "application_number": "ANDA209457", "marketing_category": "ANDA", "marketing_start_date": "20201104", "listing_expiration_date": "20261231"}