fenofibrate

Generic: fenofibrate

Labeler: westminster pharmaceuticals, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name fenofibrate
Generic Name fenofibrate
Labeler westminster pharmaceuticals, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

fenofibrate 160 mg/1

Manufacturer
Westminster Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 69367-254
Product ID 69367-254_49fd09a5-aa09-e807-e063-6294a90af3d9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207803
Listing Expiration 2027-12-31
Marketing Start 2020-04-23

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 69367254
Hyphenated Format 69367-254

Supplemental Identifiers

RxCUI
349287 351133
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 ANDA207803 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 160 mg/1
source: ndc
Packaging
  • 500 TABLET, FILM COATED in 1 BOTTLE (69367-254-05)
  • 90 TABLET, FILM COATED in 1 BOTTLE (69367-254-09)
source: ndc

Packages (2)

69367-254-05 500 TABLET, FILM COATED in 1 BOTTLE (69367-254-05) 69367-254-09 90 TABLET, FILM COATED in 1 BOTTLE (69367-254-09)

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": "49fd09a5-aa09-e807-e063-6294a90af3d9", "openfda": {"nui": ["N0000175596", "N0000175375", "M0543661"], "unii": ["U202363UOS"], "rxcui": ["349287", "351133"], "spl_set_id": ["a97ebf51-4f68-4426-9958-5c59f91b1d47"], "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": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (69367-254-05)", "package_ndc": "69367-254-05", "marketing_start_date": "20200423"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (69367-254-09)", "package_ndc": "69367-254-09", "marketing_start_date": "20200423"}], "brand_name": "Fenofibrate", "product_id": "69367-254_49fd09a5-aa09-e807-e063-6294a90af3d9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Peroxisome Proliferator Receptor alpha Agonist [EPC]"], "product_ndc": "69367-254", "generic_name": "Fenofibrate", "labeler_name": "Westminster Pharmaceuticals, LLC", "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": "20271231"}