Package 59651-217-90
Brand: fenofibric acid
Generic: fenofibric acidPackage Facts
Identity
Package NDC
59651-217-90
Digits Only
5965121790
Product NDC
59651-217
Description
90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (59651-217-90)
Marketing
Marketing Status
Brand
fenofibric acid
Generic
fenofibric acid
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "21dc5a32-9e47-415c-8b55-f97c5e7b15e1", "openfda": {"nui": ["N0000175596"], "unii": ["BGF9MN2HU1"], "rxcui": ["828373", "828379"], "spl_set_id": ["9ad201de-fa62-4c49-bc61-ee09b9ba434c"], "pharm_class_epc": ["Peroxisome Proliferator Receptor alpha Agonist [EPC]"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (59651-217-90)", "package_ndc": "59651-217-90", "marketing_start_date": "20190725"}], "brand_name": "FENOFIBRIC ACID", "product_id": "59651-217_21dc5a32-9e47-415c-8b55-f97c5e7b15e1", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Peroxisome Proliferator Receptor alpha Agonist [EPC]"], "product_ndc": "59651-217", "generic_name": "FENOFIBRIC ACID", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FENOFIBRIC ACID", "active_ingredients": [{"name": "FENOFIBRIC ACID", "strength": "135 mg/1"}], "application_number": "ANDA212598", "marketing_category": "ANDA", "marketing_start_date": "20190725", "listing_expiration_date": "20261231"}