Package 46708-555-90
Brand: fenofibrate
Generic: fenofibratePackage Facts
Identity
Package NDC
46708-555-90
Digits Only
4670855590
Product NDC
46708-555
Description
90 TABLET, FILM COATED in 1 BOTTLE (46708-555-90)
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": "037d6074-3c99-4fdc-99f0-f0b58bdbb874", "openfda": {"nui": ["N0000175596", "N0000175375", "M0543661"], "unii": ["U202363UOS"], "rxcui": ["349287", "351133"], "spl_set_id": ["39e61e9d-dda8-4989-a3dd-79545a5c9157"], "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": ["Alembic Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (46708-555-90)", "package_ndc": "46708-555-90", "marketing_start_date": "20190801"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (46708-555-91)", "package_ndc": "46708-555-91", "marketing_start_date": "20190801"}], "brand_name": "Fenofibrate", "product_id": "46708-555_037d6074-3c99-4fdc-99f0-f0b58bdbb874", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Peroxisome Proliferator Receptor alpha Agonist [EPC]"], "product_ndc": "46708-555", "generic_name": "Fenofibrate", "labeler_name": "Alembic Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fenofibrate", "active_ingredients": [{"name": "FENOFIBRATE", "strength": "160 mg/1"}], "application_number": "ANDA209660", "marketing_category": "ANDA", "marketing_start_date": "20190801", "listing_expiration_date": "20261231"}