Package 43598-267-04

Brand: icosapent

Generic: icosapent ethyl
NDC Package

Package Facts

Identity

Package NDC 43598-267-04
Digits Only 4359826704
Product NDC 43598-267
Product ID 43598-267_d6afc522-23f4-025c-df81-109460653b4d
Description

120 CAPSULE in 1 BOTTLE (43598-267-04)

Marketing

Marketing Status
Marketed Since 2021-06-21
Brand icosapent
Generic icosapent ethyl
Sample Package No

Linked Drug Pages (1)

Icosapent ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "d6afc522-23f4-025c-df81-109460653b4d", "openfda": {"unii": ["6GC8A4PAYH"], "rxcui": ["1304979"], "spl_set_id": ["1aca884c-c464-900d-ac06-33aee7118df8"], "manufacturer_name": ["Dr. Reddy's Laboratories, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 CAPSULE in 1 BOTTLE (43598-267-04)", "package_ndc": "43598-267-04", "marketing_start_date": "20210621"}], "brand_name": "Icosapent", "product_id": "43598-267_d6afc522-23f4-025c-df81-109460653b4d", "dosage_form": "CAPSULE", "product_ndc": "43598-267", "generic_name": "Icosapent Ethyl", "labeler_name": "Dr. Reddy's Laboratories, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Icosapent", "active_ingredients": [{"name": "ICOSAPENT ETHYL", "strength": "1000 mg/1"}], "application_number": "ANDA209499", "marketing_category": "ANDA", "marketing_start_date": "20210621", "listing_expiration_date": "20261231"}