Package 70710-1592-7
Brand: icosapent ethyl
Generic: icosapent ethylPackage Facts
Identity
Package NDC
70710-1592-7
Digits Only
7071015927
Product NDC
70710-1592
Description
120 CAPSULE in 1 BOTTLE (70710-1592-7)
Marketing
Marketing Status
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": "b292c3ea-8ce0-471f-8c44-57d1c4df9bf5", "openfda": {"upc": ["0370710159276"], "unii": ["6GC8A4PAYH"], "rxcui": ["1304979", "1811180"], "spl_set_id": ["5910742b-c5e6-4029-9a19-97669e3808bc"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 CAPSULE in 1 BOTTLE (70710-1592-7)", "package_ndc": "70710-1592-7", "marketing_start_date": "20230804"}], "brand_name": "icosapent ethyl", "product_id": "70710-1592_b292c3ea-8ce0-471f-8c44-57d1c4df9bf5", "dosage_form": "CAPSULE", "product_ndc": "70710-1592", "generic_name": "icosapent ethyl", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "icosapent ethyl", "active_ingredients": [{"name": "ICOSAPENT ETHYL", "strength": "1 g/1"}], "application_number": "ANDA217656", "marketing_category": "ANDA", "marketing_start_date": "20230804", "listing_expiration_date": "20261231"}