Package 59651-216-90

Brand: fenofibric acid

Generic: fenofibric acid
NDC Package

Package Facts

Identity

Package NDC 59651-216-90
Digits Only 5965121690
Product NDC 59651-216
Description

90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (59651-216-90)

Marketing

Marketing Status
Marketed Since 2019-07-25
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 (59651-216-90)", "package_ndc": "59651-216-90", "marketing_start_date": "20190725"}], "brand_name": "FENOFIBRIC ACID", "product_id": "59651-216_21dc5a32-9e47-415c-8b55-f97c5e7b15e1", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Peroxisome Proliferator Receptor alpha Agonist [EPC]"], "product_ndc": "59651-216", "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": "45 mg/1"}], "application_number": "ANDA212598", "marketing_category": "ANDA", "marketing_start_date": "20190725", "listing_expiration_date": "20261231"}