fenofibrate

Generic: fenofibrate

Labeler: camber pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name fenofibrate
Generic Name fenofibrate
Labeler camber pharmaceuticals, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

fenofibrate 48 mg/1

Manufacturer
Camber Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 31722-595
Product ID 31722-595_3a0bacd4-7a48-214e-e063-6394a90ac69f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204598
Listing Expiration 2026-12-31
Marketing Start 2016-07-14

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 31722595
Hyphenated Format 31722-595

Supplemental Identifiers

RxCUI
477560 477562
UPC
0331722596305 0331722595308
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 ANDA204598 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 48 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (31722-595-30)
  • 100 TABLET, FILM COATED in 1 BLISTER PACK (31722-595-31)
  • 100 TABLET, FILM COATED in 1 BLISTER PACK (31722-595-32)
  • 90 TABLET, FILM COATED in 1 BOTTLE (31722-595-90)
source: ndc

Packages (4)

31722-595-30 30 TABLET, FILM COATED in 1 BOTTLE (31722-595-30) 31722-595-31 100 TABLET, FILM COATED in 1 BLISTER PACK (31722-595-31) 31722-595-32 100 TABLET, FILM COATED in 1 BLISTER PACK (31722-595-32) 31722-595-90 90 TABLET, FILM COATED in 1 BOTTLE (31722-595-90)

Ingredients (1)

fenofibrate (48 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": "3a0bacd4-7a48-214e-e063-6394a90ac69f", "openfda": {"nui": ["N0000175596", "N0000175375", "M0543661"], "upc": ["0331722596305", "0331722595308"], "unii": ["U202363UOS"], "rxcui": ["477560", "477562"], "spl_set_id": ["38f43148-4ca0-402a-ba39-8ee5011a7907"], "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": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (31722-595-30)", "package_ndc": "31722-595-30", "marketing_start_date": "20160714"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BLISTER PACK (31722-595-31)", "package_ndc": "31722-595-31", "marketing_start_date": "20160714"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BLISTER PACK (31722-595-32)", "package_ndc": "31722-595-32", "marketing_start_date": "20160714"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (31722-595-90)", "package_ndc": "31722-595-90", "marketing_start_date": "20160714"}], "brand_name": "Fenofibrate", "product_id": "31722-595_3a0bacd4-7a48-214e-e063-6394a90ac69f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Peroxisome Proliferator Receptor alpha Agonist [EPC]"], "product_ndc": "31722-595", "generic_name": "Fenofibrate", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fenofibrate", "active_ingredients": [{"name": "FENOFIBRATE", "strength": "48 mg/1"}], "application_number": "ANDA204598", "marketing_category": "ANDA", "marketing_start_date": "20160714", "listing_expiration_date": "20261231"}