fenofibrate
Generic: fenofibrate
Labeler: proficient rx lpDrug Facts
Product Profile
Brand Name
fenofibrate
Generic Name
fenofibrate
Labeler
proficient rx lp
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
fenofibrate 160 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71205-949
Product ID
71205-949_7086101a-d52f-43a3-9fc3-70c2aa9487bf
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA207803
Listing Expiration
2026-12-31
Marketing Start
2020-04-23
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
71205949
Hyphenated Format
71205-949
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
ANDA207803 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 160 mg/1
Packaging
- 30 TABLET, FILM COATED in 1 BOTTLE (71205-949-30)
- 500 TABLET, FILM COATED in 1 BOTTLE (71205-949-55)
- 60 TABLET, FILM COATED in 1 BOTTLE (71205-949-60)
- 120 TABLET, FILM COATED in 1 BOTTLE (71205-949-72)
- 180 TABLET, FILM COATED in 1 BOTTLE (71205-949-78)
- 90 TABLET, FILM COATED in 1 BOTTLE (71205-949-90)
Packages (6)
71205-949-30
30 TABLET, FILM COATED in 1 BOTTLE (71205-949-30)
71205-949-55
500 TABLET, FILM COATED in 1 BOTTLE (71205-949-55)
71205-949-60
60 TABLET, FILM COATED in 1 BOTTLE (71205-949-60)
71205-949-72
120 TABLET, FILM COATED in 1 BOTTLE (71205-949-72)
71205-949-78
180 TABLET, FILM COATED in 1 BOTTLE (71205-949-78)
71205-949-90
90 TABLET, FILM COATED in 1 BOTTLE (71205-949-90)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7086101a-d52f-43a3-9fc3-70c2aa9487bf", "openfda": {"nui": ["N0000175596", "N0000175375", "M0543661"], "unii": ["U202363UOS"], "rxcui": ["349287"], "spl_set_id": ["41f0f514-1fa9-47a0-a085-a31354842f96"], "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": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71205-949-30)", "package_ndc": "71205-949-30", "marketing_start_date": "20201008"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (71205-949-55)", "package_ndc": "71205-949-55", "marketing_start_date": "20201008"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71205-949-60)", "package_ndc": "71205-949-60", "marketing_start_date": "20201008"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (71205-949-72)", "package_ndc": "71205-949-72", "marketing_start_date": "20201008"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (71205-949-78)", "package_ndc": "71205-949-78", "marketing_start_date": "20201008"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71205-949-90)", "package_ndc": "71205-949-90", "marketing_start_date": "20201008"}], "brand_name": "Fenofibrate", "product_id": "71205-949_7086101a-d52f-43a3-9fc3-70c2aa9487bf", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Peroxisome Proliferator Receptor alpha Agonist [EPC]"], "product_ndc": "71205-949", "generic_name": "Fenofibrate", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fenofibrate", "active_ingredients": [{"name": "FENOFIBRATE", "strength": "160 mg/1"}], "application_number": "ANDA207803", "marketing_category": "ANDA", "marketing_start_date": "20200423", "listing_expiration_date": "20261231"}