Package 71335-0872-1
Brand: fenofibrate
Generic: fenofibratePackage Facts
Identity
Package NDC
71335-0872-1
Digits Only
7133508721
Product NDC
71335-0872
Description
30 TABLET, FILM COATED in 1 BOTTLE (71335-0872-1)
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": "de559204-8191-4de6-93f7-b817cb6d9d6f", "openfda": {"nui": ["N0000175596", "N0000175375", "M0543661"], "unii": ["U202363UOS"], "rxcui": ["477560"], "spl_set_id": ["3db58c5c-b862-4871-b3f9-597aaeba56c4"], "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": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-0872-1)", "package_ndc": "71335-0872-1", "marketing_start_date": "20190307"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-0872-2)", "package_ndc": "71335-0872-2", "marketing_start_date": "20180620"}, {"sample": false, "description": "28 TABLET, FILM COATED in 1 BOTTLE (71335-0872-3)", "package_ndc": "71335-0872-3", "marketing_start_date": "20211227"}], "brand_name": "Fenofibrate", "product_id": "71335-0872_de559204-8191-4de6-93f7-b817cb6d9d6f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Peroxisome Proliferator Receptor alpha Agonist [EPC]"], "product_ndc": "71335-0872", "generic_name": "fenofibrate", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fenofibrate", "active_ingredients": [{"name": "FENOFIBRATE", "strength": "145 mg/1"}], "application_number": "ANDA200884", "marketing_category": "ANDA", "marketing_start_date": "20180601", "listing_expiration_date": "20261231"}