febuxostat

Generic: febuxostat

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

Drug Facts

Product Profile

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

febuxostat 80 mg/1

Manufacturer
Sun Pharmaceutical Industries, Inc.

Identifiers & Regulatory

Product NDC 47335-722
Product ID 47335-722_53dfe063-e9bf-4069-b4cc-5a83a27d18ec
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205467
Listing Expiration 2026-12-31
Marketing Start 2019-07-05

Pharmacologic Class

Established (EPC)
xanthine oxidase inhibitor [epc]
Mechanism of Action
xanthine oxidase inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 47335722
Hyphenated Format 47335-722

Supplemental Identifiers

RxCUI
834235 834241
UNII
101V0R1N2E
NUI
N0000175698 N0000000206

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 febuxostat (source: ndc)
Generic Name febuxostat (source: ndc)
Application Number ANDA205467 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 80 mg/1
source: ndc
Packaging
  • 1000 TABLET, FILM COATED in 1 BOTTLE (47335-722-18)
  • 30 TABLET, FILM COATED in 1 BOTTLE (47335-722-83)
  • 100 TABLET, FILM COATED in 1 BOTTLE (47335-722-88)
source: ndc

Packages (3)

47335-722-18 1000 TABLET, FILM COATED in 1 BOTTLE (47335-722-18) 47335-722-83 30 TABLET, FILM COATED in 1 BOTTLE (47335-722-83) 47335-722-88 100 TABLET, FILM COATED in 1 BOTTLE (47335-722-88)

Ingredients (1)

febuxostat (80 mg/1)

Linked Drug Pages (1)

Febuxostat ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "53dfe063-e9bf-4069-b4cc-5a83a27d18ec", "openfda": {"nui": ["N0000175698", "N0000000206"], "unii": ["101V0R1N2E"], "rxcui": ["834235", "834241"], "spl_set_id": ["1f7541bd-bf32-422b-b99a-89193cf193ca"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (47335-722-18)", "package_ndc": "47335-722-18", "marketing_start_date": "20190705"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (47335-722-83)", "package_ndc": "47335-722-83", "marketing_start_date": "20190705"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (47335-722-88)", "package_ndc": "47335-722-88", "marketing_start_date": "20190705"}], "brand_name": "Febuxostat", "product_id": "47335-722_53dfe063-e9bf-4069-b4cc-5a83a27d18ec", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "47335-722", "generic_name": "Febuxostat", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Febuxostat", "active_ingredients": [{"name": "FEBUXOSTAT", "strength": "80 mg/1"}], "application_number": "ANDA205467", "marketing_category": "ANDA", "marketing_start_date": "20190705", "listing_expiration_date": "20261231"}