allopurinol

Generic: allopurinol

Labeler: actavis pharma, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name allopurinol
Generic Name allopurinol
Labeler actavis pharma, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

allopurinol 100 mg/1

Manufacturer
Actavis Pharma, Inc.

Identifiers & Regulatory

Product NDC 0591-5543
Product ID 0591-5543_b7502c6f-ebdf-4d6a-aed2-93de7c6085b4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA018832
Listing Expiration 2026-12-31
Marketing Start 2009-04-06

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 05915543
Hyphenated Format 0591-5543

Supplemental Identifiers

RxCUI
197319 197320
UPC
0305915544015 0305915543018
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 NDA018832 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE, PLASTIC (0591-5543-01)
  • 1000 TABLET in 1 BOTTLE, PLASTIC (0591-5543-10)
source: ndc

Packages (2)

0591-5543-01 100 TABLET in 1 BOTTLE, PLASTIC (0591-5543-01) 0591-5543-10 1000 TABLET in 1 BOTTLE, PLASTIC (0591-5543-10)

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": "b7502c6f-ebdf-4d6a-aed2-93de7c6085b4", "openfda": {"nui": ["N0000175698", "N0000000206"], "upc": ["0305915544015", "0305915543018"], "unii": ["63CZ7GJN5I"], "rxcui": ["197319", "197320"], "spl_set_id": ["a80fe56f-8d03-423f-8e2a-7ec8c9e5045b"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (0591-5543-01)", "package_ndc": "0591-5543-01", "marketing_start_date": "20090406"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (0591-5543-10)", "package_ndc": "0591-5543-10", "marketing_start_date": "20090406"}], "brand_name": "Allopurinol", "product_id": "0591-5543_b7502c6f-ebdf-4d6a-aed2-93de7c6085b4", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "0591-5543", "generic_name": "Allopurinol", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Allopurinol", "active_ingredients": [{"name": "ALLOPURINOL", "strength": "100 mg/1"}], "application_number": "NDA018832", "marketing_category": "NDA", "marketing_start_date": "20090406", "listing_expiration_date": "20261231"}