allopurinol

Generic: allopurinol

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

Drug Facts

Product Profile

Brand Name allopurinol
Generic Name allopurinol
Labeler nucare pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

allopurinol 100 mg/1

Manufacturer
NuCare Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 66267-665
Product ID 66267-665_1fa77d0a-40f1-b54e-e063-6294a90a0375
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203154
Listing Expiration 2026-12-31
Marketing Start 2015-04-29

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 66267665
Hyphenated Format 66267-665

Supplemental Identifiers

RxCUI
197319
UPC
0366267665902
UNII
63CZ7GJN5I
NUI
N0000175698 N0000000206

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 allopurinol (source: ndc)
Generic Name allopurinol (source: ndc)
Application Number ANDA203154 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (66267-665-30)
  • 60 TABLET in 1 BOTTLE (66267-665-60)
  • 90 TABLET in 1 BOTTLE (66267-665-90)
source: ndc

Packages (3)

66267-665-30 30 TABLET in 1 BOTTLE (66267-665-30) 66267-665-60 60 TABLET in 1 BOTTLE (66267-665-60) 66267-665-90 90 TABLET in 1 BOTTLE (66267-665-90)

Ingredients (1)

allopurinol (100 mg/1)

Linked Drug Pages (1)

Allopurinol ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1fa77d0a-40f1-b54e-e063-6294a90a0375", "openfda": {"nui": ["N0000175698", "N0000000206"], "upc": ["0366267665902"], "unii": ["63CZ7GJN5I"], "rxcui": ["197319"], "spl_set_id": ["44bcc8df-a803-010f-e054-00144ff88e88"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (66267-665-30)", "package_ndc": "66267-665-30", "marketing_start_date": "20161228"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (66267-665-60)", "package_ndc": "66267-665-60", "marketing_start_date": "20161228"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (66267-665-90)", "package_ndc": "66267-665-90", "marketing_start_date": "20161228"}], "brand_name": "Allopurinol", "product_id": "66267-665_1fa77d0a-40f1-b54e-e063-6294a90a0375", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "66267-665", "generic_name": "allopurinol", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Allopurinol", "active_ingredients": [{"name": "ALLOPURINOL", "strength": "100 mg/1"}], "application_number": "ANDA203154", "marketing_category": "ANDA", "marketing_start_date": "20150429", "listing_expiration_date": "20261231"}