Package 51655-856-52
Brand: fenofibrate
Generic: fenofibratePackage Facts
Identity
Package NDC
51655-856-52
Digits Only
5165585652
Product NDC
51655-856
Description
30 TABLET in 1 BOTTLE, PLASTIC (51655-856-52)
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": "4973f1bb-8ce9-3708-e063-6294a90a33d5", "openfda": {"nui": ["N0000175596", "N0000175375", "M0543661"], "unii": ["U202363UOS"], "rxcui": ["349287"], "spl_set_id": ["f7590970-c54d-24e9-e053-6294a90ac400"], "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": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-856-52)", "package_ndc": "51655-856-52", "marketing_start_date": "20230213"}], "brand_name": "FENOFIBRATE", "product_id": "51655-856_4973f1bb-8ce9-3708-e063-6294a90a33d5", "dosage_form": "TABLET", "pharm_class": ["Peroxisome Proliferator Receptor alpha Agonist [EPC]"], "product_ndc": "51655-856", "generic_name": "FENOFIBRATE", "labeler_name": "Northwind Health Company, 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": "20230213", "listing_expiration_date": "20271231"}