allopurinol

Generic: allopurinol

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name allopurinol
Generic Name allopurinol
Labeler direct_rx
Dosage Form TABLET
Routes
ORAL
Active Ingredients

allopurinol 300 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 72189-417
Product ID 72189-417_4c4bb472-bcf4-c5df-e063-6394a90a787d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204467
Marketing Start 2023-02-02
Marketing End 2029-10-31

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 72189417
Hyphenated Format 72189-417

Supplemental Identifiers

RxCUI
197320
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 ANDA204467 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 300 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (72189-417-30)
  • 90 TABLET in 1 BOTTLE (72189-417-90)
source: ndc

Packages (2)

72189-417-30 30 TABLET in 1 BOTTLE (72189-417-30) 72189-417-90 90 TABLET in 1 BOTTLE (72189-417-90)

Ingredients (1)

allopurinol (300 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": "4c4bb472-bcf4-c5df-e063-6394a90a787d", "openfda": {"nui": ["N0000175698", "N0000000206"], "unii": ["63CZ7GJN5I"], "rxcui": ["197320"], "spl_set_id": ["f3bd5852-8e43-6b5d-e053-2995a90a194f"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-417-30)", "package_ndc": "72189-417-30", "marketing_end_date": "20291031", "marketing_start_date": "20230202"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (72189-417-90)", "package_ndc": "72189-417-90", "marketing_end_date": "20291031", "marketing_start_date": "20230202"}], "brand_name": "ALLOPURINOL", "product_id": "72189-417_4c4bb472-bcf4-c5df-e063-6394a90a787d", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "72189-417", "generic_name": "ALLOPURINOL", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ALLOPURINOL", "active_ingredients": [{"name": "ALLOPURINOL", "strength": "300 mg/1"}], "application_number": "ANDA204467", "marketing_category": "ANDA", "marketing_end_date": "20291031", "marketing_start_date": "20230202"}