Package 72603-841-02
Brand: fenofibrate
Generic: fenofibratePackage Facts
Identity
Package NDC
72603-841-02
Digits Only
7260384102
Product NDC
72603-841
Description
500 TABLET in 1 BOTTLE (72603-841-02)
Marketing
Marketing Status
Brand
fenofibrate
Generic
fenofibrate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "14f18477-a8d7-4aea-82cb-f0100e6c24a5", "openfda": {"nui": ["N0000175596", "N0000175375", "M0543661"], "upc": ["0372603841022"], "unii": ["U202363UOS"], "rxcui": ["349287", "351133"], "spl_set_id": ["3b448774-aebf-45fe-92f1-b8eca53cf09b"], "pharm_class_cs": ["Fibric Acids [CS]"], "pharm_class_epc": ["Peroxisome Proliferator Receptor alpha Agonist [EPC]"], "pharm_class_moa": ["Peroxisome Proliferator-activated Receptor alpha Agonists [MoA]"], "manufacturer_name": ["NorthStar RxLLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (72603-841-01)", "package_ndc": "72603-841-01", "marketing_start_date": "20250929"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (72603-841-02)", "package_ndc": "72603-841-02", "marketing_start_date": "20250929"}], "brand_name": "FENOFIBRATE", "product_id": "72603-841_14f18477-a8d7-4aea-82cb-f0100e6c24a5", "dosage_form": "TABLET", "pharm_class": ["Peroxisome Proliferator Receptor alpha Agonist [EPC]"], "product_ndc": "72603-841", "generic_name": "FENOFIBRATE", "labeler_name": "NorthStar RxLLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FENOFIBRATE", "active_ingredients": [{"name": "FENOFIBRATE", "strength": "160 mg/1"}], "application_number": "ANDA213864", "marketing_category": "ANDA", "marketing_start_date": "20250929", "listing_expiration_date": "20261231"}