fenofibrate

Generic: fenofibrate

Labeler: laurus labs limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name fenofibrate
Generic Name fenofibrate
Labeler laurus labs limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

fenofibrate 145 mg/1

Manufacturer
Laurus Labs Limited

Identifiers & Regulatory

Product NDC 42385-951
Product ID 42385-951_f0dd74ce-5a8e-07b1-e053-2a95a90af387
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211122
Listing Expiration 2026-12-31
Marketing Start 2020-03-18

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 42385951
Hyphenated Format 42385-951

Supplemental Identifiers

RxCUI
477560 477562
UNII
U202363UOS
NUI
N0000175596 N0000175375 M0543661

Packaging Origin

Original Packager
true

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 ANDA211122 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 145 mg/1
source: ndc
Packaging
  • 1000 TABLET in 1 BOTTLE (42385-951-11)
  • 30 TABLET in 1 BOTTLE (42385-951-30)
  • 90 TABLET in 1 BOTTLE (42385-951-90)
source: ndc

Packages (3)

42385-951-11 1000 TABLET in 1 BOTTLE (42385-951-11) 42385-951-30 30 TABLET in 1 BOTTLE (42385-951-30) 42385-951-90 90 TABLET in 1 BOTTLE (42385-951-90)

Ingredients (1)

fenofibrate (145 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": "f0dd74ce-5a8e-07b1-e053-2a95a90af387", "openfda": {"nui": ["N0000175596", "N0000175375", "M0543661"], "unii": ["U202363UOS"], "rxcui": ["477560", "477562"], "spl_set_id": ["0da6d56e-1ed6-437d-b88d-16b014d1889a"], "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": ["Laurus Labs Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (42385-951-11)", "package_ndc": "42385-951-11", "marketing_start_date": "20200318"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (42385-951-30)", "package_ndc": "42385-951-30", "marketing_start_date": "20200318"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (42385-951-90)", "package_ndc": "42385-951-90", "marketing_start_date": "20200318"}], "brand_name": "fenofibrate", "product_id": "42385-951_f0dd74ce-5a8e-07b1-e053-2a95a90af387", "dosage_form": "TABLET", "pharm_class": ["Peroxisome Proliferator Receptor alpha Agonist [EPC]"], "product_ndc": "42385-951", "generic_name": "fenofibrate", "labeler_name": "Laurus Labs Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "fenofibrate", "active_ingredients": [{"name": "FENOFIBRATE", "strength": "145 mg/1"}], "application_number": "ANDA211122", "marketing_category": "ANDA", "marketing_start_date": "20200318", "listing_expiration_date": "20261231"}