fenofibrate

Generic: fenofibrate

Labeler: trifluent pharma llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name fenofibrate
Generic Name fenofibrate
Labeler trifluent pharma llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

fenofibrate 120 mg/1

Manufacturer
Trifluent Pharma LLC

Identifiers & Regulatory

Product NDC 73352-102
Product ID 73352-102_3c3539f7-7a1e-8fd3-e063-6294a90a1082
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217732
Listing Expiration 2026-12-31
Marketing Start 2025-08-12

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 73352102
Hyphenated Format 73352-102

Supplemental Identifiers

RxCUI
749802 749804
UPC
0373352101016 0373352102013
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 ANDA217732 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 120 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (73352-102-01)
source: ndc

Packages (1)

Ingredients (1)

fenofibrate (120 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3c3539f7-7a1e-8fd3-e063-6294a90a1082", "openfda": {"nui": ["N0000175596", "N0000175375", "M0543661"], "upc": ["0373352101016", "0373352102013"], "unii": ["U202363UOS"], "rxcui": ["749802", "749804"], "spl_set_id": ["3c3539e4-bc4a-8152-e063-6294a90ab55c"], "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": ["Trifluent Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (73352-102-01)", "package_ndc": "73352-102-01", "marketing_start_date": "20250812"}], "brand_name": "FENOFIBRATE", "product_id": "73352-102_3c3539f7-7a1e-8fd3-e063-6294a90a1082", "dosage_form": "TABLET", "pharm_class": ["Peroxisome Proliferator Receptor alpha Agonist [EPC]"], "product_ndc": "73352-102", "generic_name": "fenofibrate", "labeler_name": "Trifluent Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FENOFIBRATE", "active_ingredients": [{"name": "FENOFIBRATE", "strength": "120 mg/1"}], "application_number": "ANDA217732", "marketing_category": "ANDA", "marketing_start_date": "20250812", "listing_expiration_date": "20261231"}