Package 70756-215-51
Brand: fenofibrate
Generic: fenofibratePackage Facts
Identity
Package NDC
70756-215-51
Digits Only
7075621551
Product NDC
70756-215
Description
500 TABLET in 1 BOTTLE (70756-215-51)
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": "4a13e20b-6a21-4d45-a159-a2add4ce215e", "openfda": {"nui": ["N0000175596", "N0000175375", "M0543661"], "upc": ["0370756215516"], "unii": ["U202363UOS"], "rxcui": ["349287", "351133"], "spl_set_id": ["1da57e8c-3977-43e1-aa7e-229760203f7d"], "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": ["Lifestar Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (70756-215-51)", "package_ndc": "70756-215-51", "marketing_start_date": "20200910"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (70756-215-90)", "package_ndc": "70756-215-90", "marketing_start_date": "20200910"}], "brand_name": "FENOFIBRATE", "product_id": "70756-215_4a13e20b-6a21-4d45-a159-a2add4ce215e", "dosage_form": "TABLET", "pharm_class": ["Peroxisome Proliferator Receptor alpha Agonist [EPC]"], "product_ndc": "70756-215", "generic_name": "FENOFIBRATE", "labeler_name": "Lifestar Pharma LLC", "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": "20200910", "listing_expiration_date": "20261231"}