Package 72865-290-12

Brand: icosapent ethyl

Generic: icosapent ethyl
NDC Package

Package Facts

Identity

Package NDC 72865-290-12
Digits Only 7286529012
Product NDC 72865-290
Description

120 CAPSULE in 1 BOTTLE (72865-290-12)

Marketing

Marketing Status
Marketed Since 2024-02-16
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": "fc2e665c-7b0e-4969-998e-be05e0e73520", "openfda": {"upc": ["0372865290125", "0372865289242"], "unii": ["6GC8A4PAYH"], "rxcui": ["1304979", "1811180"], "spl_set_id": ["019cc0ac-0c2f-426d-996a-6d932f954443"], "manufacturer_name": ["XLCare Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 CAPSULE in 1 BOTTLE (72865-290-12)", "package_ndc": "72865-290-12", "marketing_start_date": "20240216"}], "brand_name": "ICOSAPENT ETHYL", "product_id": "72865-290_fc2e665c-7b0e-4969-998e-be05e0e73520", "dosage_form": "CAPSULE", "product_ndc": "72865-290", "generic_name": "Icosapent ethyl", "labeler_name": "XLCare Pharmaceuticals, Inc.", "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": "20240216", "listing_expiration_date": "20261231"}