fenofibrate

Generic: fenofibrate

Labeler: amneal pharmaceuticals ny llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name fenofibrate
Generic Name fenofibrate
Labeler amneal pharmaceuticals ny llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

fenofibrate 145 mg/1

Manufacturer
Amneal Pharmaceuticals NY LLC

Identifiers & Regulatory

Product NDC 69238-1261
Product ID 69238-1261_3c74b751-6125-4600-a38b-20eb97bbad16
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209951
Listing Expiration 2026-12-31
Marketing Start 2018-02-15

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 692381261
Hyphenated Format 69238-1261

Supplemental Identifiers

RxCUI
477560 477562
UPC
0369238126198 0369238126099
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 ANDA209951 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 145 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (69238-1261-9)
source: ndc

Packages (1)

Ingredients (1)

fenofibrate (145 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3c74b751-6125-4600-a38b-20eb97bbad16", "openfda": {"nui": ["N0000175596", "N0000175375", "M0543661"], "upc": ["0369238126198", "0369238126099"], "unii": ["U202363UOS"], "rxcui": ["477560", "477562"], "spl_set_id": ["283e754e-6ffa-4d6a-882f-9bbb3cbc8ca8"], "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": ["Amneal Pharmaceuticals NY LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (69238-1261-9)", "package_ndc": "69238-1261-9", "marketing_start_date": "20180215"}], "brand_name": "Fenofibrate", "product_id": "69238-1261_3c74b751-6125-4600-a38b-20eb97bbad16", "dosage_form": "TABLET", "pharm_class": ["Peroxisome Proliferator Receptor alpha Agonist [EPC]"], "product_ndc": "69238-1261", "generic_name": "Fenofibrate", "labeler_name": "Amneal Pharmaceuticals NY LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fenofibrate", "active_ingredients": [{"name": "FENOFIBRATE", "strength": "145 mg/1"}], "application_number": "ANDA209951", "marketing_category": "ANDA", "marketing_start_date": "20180215", "listing_expiration_date": "20261231"}