allopurinol

Generic: allopurinol

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

Drug Facts

Product Profile

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

allopurinol 100 mg/1

Manufacturer
XLCare Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 72865-303
Product ID 72865-303_47dd9bd8-06e7-b387-e063-6294a90a74d4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217748
Listing Expiration 2027-12-31
Marketing Start 2026-01-08

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 72865303
Hyphenated Format 72865-303

Supplemental Identifiers

RxCUI
197319 197320
UPC
0372865304907 0372865303900
UNII
63CZ7GJN5I
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 allopurinol (source: ndc)
Generic Name allopurinol (source: ndc)
Application Number ANDA217748 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (72865-303-01)
  • 500 TABLET in 1 BOTTLE (72865-303-05)
  • 1000 TABLET in 1 BOTTLE (72865-303-10)
  • 90 TABLET in 1 BOTTLE (72865-303-90)
source: ndc

Packages (4)

72865-303-01 100 TABLET in 1 BOTTLE (72865-303-01) 72865-303-05 500 TABLET in 1 BOTTLE (72865-303-05) 72865-303-10 1000 TABLET in 1 BOTTLE (72865-303-10) 72865-303-90 90 TABLET in 1 BOTTLE (72865-303-90)

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": "47dd9bd8-06e7-b387-e063-6294a90a74d4", "openfda": {"nui": ["N0000175698", "N0000000206"], "upc": ["0372865304907", "0372865303900"], "unii": ["63CZ7GJN5I"], "rxcui": ["197319", "197320"], "spl_set_id": ["fc7973c8-d846-4eca-ab0d-d30228035ba2"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["XLCare Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72865-303-01)", "package_ndc": "72865-303-01", "marketing_start_date": "20260108"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (72865-303-05)", "package_ndc": "72865-303-05", "marketing_start_date": "20260108"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (72865-303-10)", "package_ndc": "72865-303-10", "marketing_start_date": "20260108"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (72865-303-90)", "package_ndc": "72865-303-90", "marketing_start_date": "20260108"}], "brand_name": "ALLOPURINOL", "product_id": "72865-303_47dd9bd8-06e7-b387-e063-6294a90a74d4", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "72865-303", "generic_name": "ALLOPURINOL", "labeler_name": "XLCare Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ALLOPURINOL", "active_ingredients": [{"name": "ALLOPURINOL", "strength": "100 mg/1"}], "application_number": "ANDA217748", "marketing_category": "ANDA", "marketing_start_date": "20260108", "listing_expiration_date": "20271231"}