Package 0115-1555-10
Brand: fenofibric acid
Generic: fenofibric acidPackage Facts
Identity
Package NDC
0115-1555-10
Digits Only
0115155510
Product NDC
0115-1555
Description
90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0115-1555-10)
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": "72e2c9bb-63d6-4a3b-bee1-52a18e95bf0a", "openfda": {"nui": ["N0000175596"], "unii": ["BGF9MN2HU1"], "rxcui": ["828373", "828379"], "spl_set_id": ["369b3e55-2c05-d879-fe7e-91296c529ae9"], "pharm_class_epc": ["Peroxisome Proliferator Receptor alpha Agonist [EPC]"], "manufacturer_name": ["Amneal Pharmaceuticals of New York LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0115-1555-10)", "package_ndc": "0115-1555-10", "marketing_end_date": "20260731", "marketing_start_date": "20160912"}], "brand_name": "Fenofibric Acid", "product_id": "0115-1555_72e2c9bb-63d6-4a3b-bee1-52a18e95bf0a", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Peroxisome Proliferator Receptor alpha Agonist [EPC]"], "product_ndc": "0115-1555", "generic_name": "Fenofibric Acid", "labeler_name": "Amneal Pharmaceuticals of New York LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fenofibric Acid", "active_ingredients": [{"name": "FENOFIBRIC ACID", "strength": "135 mg/1"}], "application_number": "NDA022224", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_end_date": "20260731", "marketing_start_date": "20160912"}