fenofibrate

Generic: fenofibrate

Labeler: sun pharmaceutical industries, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name fenofibrate
Generic Name fenofibrate
Labeler sun pharmaceutical industries, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

fenofibrate 145 mg/1

Manufacturer
Sun Pharmaceutical Industries, Inc.

Identifiers & Regulatory

Product NDC 63304-449
Product ID 63304-449_2cd2c807-d4f7-51da-e063-6294a90a9a63
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA200884
Listing Expiration 2026-12-31
Marketing Start 2018-06-01

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 63304449
Hyphenated Format 63304-449

Supplemental Identifiers

RxCUI
477560 477562
UPC
0363304448054 0363304449051
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 ANDA200884 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 145 mg/1
source: ndc
Packaging
  • 500 TABLET, FILM COATED in 1 BOTTLE (63304-449-05)
  • 30 TABLET, FILM COATED in 1 BOTTLE (63304-449-30)
  • 90 TABLET, FILM COATED in 1 BOTTLE (63304-449-90)
source: ndc

Packages (3)

63304-449-05 500 TABLET, FILM COATED in 1 BOTTLE (63304-449-05) 63304-449-30 30 TABLET, FILM COATED in 1 BOTTLE (63304-449-30) 63304-449-90 90 TABLET, FILM COATED in 1 BOTTLE (63304-449-90)

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": "2cd2c807-d4f7-51da-e063-6294a90a9a63", "openfda": {"nui": ["N0000175596", "N0000175375", "M0543661"], "upc": ["0363304448054", "0363304449051"], "unii": ["U202363UOS"], "rxcui": ["477560", "477562"], "spl_set_id": ["125bbd7e-86a2-4209-90a5-ad353e572d1b"], "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": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (63304-449-05)", "package_ndc": "63304-449-05", "marketing_start_date": "20180601"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (63304-449-30)", "package_ndc": "63304-449-30", "marketing_start_date": "20180601"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (63304-449-90)", "package_ndc": "63304-449-90", "marketing_start_date": "20180601"}], "brand_name": "Fenofibrate", "product_id": "63304-449_2cd2c807-d4f7-51da-e063-6294a90a9a63", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Peroxisome Proliferator Receptor alpha Agonist [EPC]"], "product_ndc": "63304-449", "generic_name": "fenofibrate", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fenofibrate", "active_ingredients": [{"name": "FENOFIBRATE", "strength": "145 mg/1"}], "application_number": "ANDA200884", "marketing_category": "ANDA", "marketing_start_date": "20180601", "listing_expiration_date": "20261231"}