fenofibrate

Generic: fenofibrate

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name fenofibrate
Generic Name fenofibrate
Labeler bryant ranch prepack
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

fenofibrate 160 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-0741
Product ID 71335-0741_01c33ccd-f3ff-40c4-901e-fecc9b1c7791
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076433
Listing Expiration 2026-12-31
Marketing Start 2017-06-01

Pharmacologic Class

Established (EPC)
peroxisome proliferator receptor alpha agonist [epc]
Mechanism of Action
peroxisome proliferator-activated receptor alpha agonists [moa]
Chemical Structure
fibric acids [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713350741
Hyphenated Format 71335-0741

Supplemental Identifiers

RxCUI
349287
UNII
U202363UOS
NUI
N0000175596 N0000175375 M0543661

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 ANDA076433 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 160 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (71335-0741-1)
  • 90 TABLET, FILM COATED in 1 BOTTLE (71335-0741-2)
  • 60 TABLET, FILM COATED in 1 BOTTLE (71335-0741-3)
  • 28 TABLET, FILM COATED in 1 BOTTLE (71335-0741-4)
  • 100 TABLET, FILM COATED in 1 BOTTLE (71335-0741-5)
source: ndc

Packages (5)

71335-0741-1 30 TABLET, FILM COATED in 1 BOTTLE (71335-0741-1) 71335-0741-2 90 TABLET, FILM COATED in 1 BOTTLE (71335-0741-2) 71335-0741-3 60 TABLET, FILM COATED in 1 BOTTLE (71335-0741-3) 71335-0741-4 28 TABLET, FILM COATED in 1 BOTTLE (71335-0741-4) 71335-0741-5 100 TABLET, FILM COATED in 1 BOTTLE (71335-0741-5)

Ingredients (1)

fenofibrate (160 mg/1)

Linked Drug Pages (1)

Fenofibrate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "01c33ccd-f3ff-40c4-901e-fecc9b1c7791", "openfda": {"nui": ["N0000175596", "N0000175375", "M0543661"], "unii": ["U202363UOS"], "rxcui": ["349287"], "spl_set_id": ["40ca5d88-6403-4c4b-ae7f-ae8cec4d9965"], "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": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-0741-1)", "package_ndc": "71335-0741-1", "marketing_start_date": "20180316"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-0741-2)", "package_ndc": "71335-0741-2", "marketing_start_date": "20180316"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-0741-3)", "package_ndc": "71335-0741-3", "marketing_start_date": "20211227"}, {"sample": false, "description": "28 TABLET, FILM COATED in 1 BOTTLE (71335-0741-4)", "package_ndc": "71335-0741-4", "marketing_start_date": "20211227"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (71335-0741-5)", "package_ndc": "71335-0741-5", "marketing_start_date": "20211227"}], "brand_name": "Fenofibrate", "product_id": "71335-0741_01c33ccd-f3ff-40c4-901e-fecc9b1c7791", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Peroxisome Proliferator Receptor alpha Agonist [EPC]"], "product_ndc": "71335-0741", "generic_name": "Fenofibrate", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fenofibrate", "active_ingredients": [{"name": "FENOFIBRATE", "strength": "160 mg/1"}], "application_number": "ANDA076433", "marketing_category": "ANDA", "marketing_start_date": "20170601", "listing_expiration_date": "20261231"}