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 100 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 72189-437
Product ID 72189-437_4c4b2794-40b6-34c5-e063-6394a90acee6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211820
Listing Expiration 2027-12-31
Marketing Start 2023-03-13

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 72189437
Hyphenated Format 72189-437

Supplemental Identifiers

RxCUI
197319
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 ANDA211820 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (72189-437-30)
  • 90 TABLET in 1 BOTTLE (72189-437-90)
source: ndc

Packages (2)

72189-437-30 30 TABLET in 1 BOTTLE (72189-437-30) 72189-437-90 90 TABLET in 1 BOTTLE (72189-437-90)

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": "4c4b2794-40b6-34c5-e063-6394a90acee6", "openfda": {"nui": ["N0000175698", "N0000000206"], "unii": ["63CZ7GJN5I"], "rxcui": ["197319"], "spl_set_id": ["f6c83ee9-c07b-9fc8-e053-6394a90a2160"], "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 (72189-437-30)", "package_ndc": "72189-437-30", "marketing_start_date": "20230313"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (72189-437-90)", "package_ndc": "72189-437-90", "marketing_start_date": "20230313"}], "brand_name": "Allopurinol", "product_id": "72189-437_4c4b2794-40b6-34c5-e063-6394a90acee6", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "72189-437", "generic_name": "Allopurinol", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Allopurinol", "active_ingredients": [{"name": "ALLOPURINOL", "strength": "100 mg/1"}], "application_number": "ANDA211820", "marketing_category": "ANDA", "marketing_start_date": "20230313", "listing_expiration_date": "20271231"}