Package 69680-186-92

Brand: icosapent ethyl

Generic: icosapent ethyl
NDC Package

Package Facts

Identity

Package NDC 69680-186-92
Digits Only 6968018692
Product NDC 69680-186
Description

120 CAPSULE in 1 BOTTLE (69680-186-92)

Marketing

Marketing Status
Marketed Since 2025-10-20
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": "cd69c4f4-24bc-4a95-89af-8afacbed1d08", "openfda": {"upc": ["0369680186924"], "unii": ["6GC8A4PAYH"], "rxcui": ["1304979"], "spl_set_id": ["4c3e26d6-9297-42ad-94b4-04e394155b41"], "manufacturer_name": ["Vitruvias Therapeutics, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 CAPSULE in 1 BOTTLE (69680-186-92)", "package_ndc": "69680-186-92", "marketing_start_date": "20251020"}], "brand_name": "Icosapent Ethyl", "product_id": "69680-186_cd69c4f4-24bc-4a95-89af-8afacbed1d08", "dosage_form": "CAPSULE", "product_ndc": "69680-186", "generic_name": "Icosapent Ethyl", "labeler_name": "Vitruvias Therapeutics, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Icosapent Ethyl", "active_ingredients": [{"name": "ICOSAPENT ETHYL", "strength": "1 g/1"}], "application_number": "ANDA219156", "marketing_category": "ANDA", "marketing_start_date": "20251020", "listing_expiration_date": "20261231"}