Package 16714-636-01

Brand: icosapent ethyl

Generic: icosapent ethyl
NDC Package

Package Facts

Identity

Package NDC 16714-636-01
Digits Only 1671463601
Product NDC 16714-636
Product ID 16714-636_ad34781b-7624-4344-a31f-83ef471da07b
Description

120 CAPSULE in 1 BOTTLE (16714-636-01)

Marketing

Marketing Status
Marketed Since 2025-07-01
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": "ad34781b-7624-4344-a31f-83ef471da07b", "openfda": {"upc": ["0316714636016"], "unii": ["6GC8A4PAYH"], "rxcui": ["1304979"], "spl_set_id": ["b5b0b1ae-29ab-43a5-9e6d-24374d961399"], "manufacturer_name": ["Northstar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 CAPSULE in 1 BOTTLE (16714-636-01)", "package_ndc": "16714-636-01", "marketing_start_date": "20250701"}], "brand_name": "ICOSAPENT ETHYL", "product_id": "16714-636_ad34781b-7624-4344-a31f-83ef471da07b", "dosage_form": "CAPSULE", "product_ndc": "16714-636", "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": "ANDA216811", "marketing_category": "ANDA", "marketing_start_date": "20250701", "listing_expiration_date": "20261231"}