fenofibrate
Generic: fenofibrate
Labeler: preferred pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
fenofibrate
Generic Name
fenofibrate
Labeler
preferred pharmaceuticals inc.
Dosage Form
TABLET
Routes
Active Ingredients
fenofibrate 145 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68788-4006
Product ID
68788-4006_2e6711e9-782d-46bd-9447-6612fe7d0fe7
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA090856
Listing Expiration
2026-12-31
Marketing Start
2025-08-08
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
687884006
Hyphenated Format
68788-4006
Supplemental Identifiers
RxCUI
UNII
NUI
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
fenofibrate (source: ndc)
Generic Name
fenofibrate (source: ndc)
Application Number
ANDA090856 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 145 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (68788-4006-1)
- 30 TABLET in 1 BOTTLE (68788-4006-3)
- 60 TABLET in 1 BOTTLE (68788-4006-6)
- 90 TABLET in 1 BOTTLE (68788-4006-9)
Packages (4)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2e6711e9-782d-46bd-9447-6612fe7d0fe7", "openfda": {"nui": ["N0000175596", "N0000175375", "M0543661"], "unii": ["U202363UOS"], "rxcui": ["477560"], "spl_set_id": ["2e6711e9-782d-46bd-9447-6612fe7d0fe7"], "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": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68788-4006-1)", "package_ndc": "68788-4006-1", "marketing_start_date": "20250808"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-4006-3)", "package_ndc": "68788-4006-3", "marketing_start_date": "20250808"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68788-4006-6)", "package_ndc": "68788-4006-6", "marketing_start_date": "20250808"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-4006-9)", "package_ndc": "68788-4006-9", "marketing_start_date": "20250808"}], "brand_name": "Fenofibrate", "product_id": "68788-4006_2e6711e9-782d-46bd-9447-6612fe7d0fe7", "dosage_form": "TABLET", "pharm_class": ["Peroxisome Proliferator Receptor alpha Agonist [EPC]"], "product_ndc": "68788-4006", "generic_name": "Fenofibrate", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fenofibrate", "active_ingredients": [{"name": "FENOFIBRATE", "strength": "145 mg/1"}], "application_number": "ANDA090856", "marketing_category": "ANDA", "marketing_start_date": "20250808", "listing_expiration_date": "20261231"}