Package 0480-0126-49

Brand: icosapent ethyl

Generic: icosapent ethyl
NDC Package

Package Facts

Identity

Package NDC 0480-0126-49
Digits Only 0480012649
Product NDC 0480-0126
Product ID 0480-0126_0d2afdd4-3333-47dc-9653-0b63e478b36d
Description

240 CAPSULE, LIQUID FILLED in 1 BOTTLE (0480-0126-49)

Marketing

Marketing Status
Marketed Since 2022-09-09
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": "0d2afdd4-3333-47dc-9653-0b63e478b36d", "openfda": {"unii": ["6GC8A4PAYH"], "rxcui": ["1304979", "1811180"], "spl_set_id": ["de7049ae-d1d6-4267-a93b-dd5039c50c2c"], "manufacturer_name": ["Teva Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "240 CAPSULE, LIQUID FILLED in 1 BOTTLE (0480-0126-49)", "package_ndc": "0480-0126-49", "marketing_start_date": "20220909"}], "brand_name": "Icosapent Ethyl", "product_id": "0480-0126_0d2afdd4-3333-47dc-9653-0b63e478b36d", "dosage_form": "CAPSULE, LIQUID FILLED", "product_ndc": "0480-0126", "generic_name": "Icosapent Ethyl", "labeler_name": "Teva Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Icosapent Ethyl", "active_ingredients": [{"name": "ICOSAPENT ETHYL", "strength": "500 mg/1"}], "application_number": "ANDA209525", "marketing_category": "ANDA", "marketing_start_date": "20220909", "listing_expiration_date": "20261231"}