Package 35916-1738-1

Brand: icosapent ethyl

Generic: icosapent ethyl
NDC Package

Package Facts

Identity

Package NDC 35916-1738-1
Digits Only 3591617381
Product NDC 35916-1738
Product ID 35916-1738_51ab40c9-9b15-4fa3-a355-6ac5d36552ee
Description

240 CAPSULE in 1 BOTTLE (35916-1738-1)

Marketing

Marketing Status
Marketed Since 2025-03-01
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": "51ab40c9-9b15-4fa3-a355-6ac5d36552ee", "openfda": {"unii": ["6GC8A4PAYH"], "rxcui": ["1304979", "1811180"], "spl_set_id": ["6f5838cd-4d17-401d-8e2a-652d0e73c1e9"], "manufacturer_name": ["Softgel Healthcare Private Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "240 CAPSULE in 1 BOTTLE (35916-1738-1)", "package_ndc": "35916-1738-1", "marketing_start_date": "20250301"}], "brand_name": "icosapent ethyl", "product_id": "35916-1738_51ab40c9-9b15-4fa3-a355-6ac5d36552ee", "dosage_form": "CAPSULE", "product_ndc": "35916-1738", "generic_name": "icosapent ethyl", "labeler_name": "Softgel Healthcare Private Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "icosapent ethyl", "active_ingredients": [{"name": "ICOSAPENT ETHYL", "strength": ".5 g/1"}], "application_number": "ANDA217656", "marketing_category": "ANDA", "marketing_start_date": "20250301", "listing_expiration_date": "20261231"}