allopurinol sodium

Generic: allopurinol sodium

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

Drug Facts

Product Profile

Brand Name allopurinol sodium
Generic Name allopurinol sodium
Labeler hikma pharmaceuticals usa inc.
Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
INTRAVENOUS
Active Ingredients

allopurinol sodium 500 mg/25mL

Manufacturer
Hikma Pharmaceuticals USA Inc.

Identifiers & Regulatory

Product NDC 0143-9533
Product ID 0143-9533_5f7a1da9-2b25-46d2-8b6b-fdb44a4e1fd7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076870
Listing Expiration 2026-12-31
Marketing Start 2004-09-01

Pharmacologic Class

Classes
xanthine oxidase inhibitor [epc] xanthine oxidase inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 01439533
Hyphenated Format 0143-9533

Supplemental Identifiers

RxCUI
252931
UNII
428673RC2Z

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 sodium (source: ndc)
Generic Name allopurinol sodium (source: ndc)
Application Number ANDA076870 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 500 mg/25mL
source: ndc
Packaging
  • 1 VIAL in 1 BOX, UNIT-DOSE (0143-9533-01) / 25 mL in 1 VIAL
source: ndc

Packages (1)

0143-9533-01 1 VIAL in 1 BOX, UNIT-DOSE (0143-9533-01) / 25 mL in 1 VIAL

Ingredients (1)

allopurinol sodium (500 mg/25mL)

Linked Drug Pages (1)

Allopurinol sodium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "5f7a1da9-2b25-46d2-8b6b-fdb44a4e1fd7", "openfda": {"unii": ["428673RC2Z"], "rxcui": ["252931"], "spl_set_id": ["9ae58f3c-dbf9-4c10-9b79-233b10e0e9f1"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BOX, UNIT-DOSE (0143-9533-01)  / 25 mL in 1 VIAL", "package_ndc": "0143-9533-01", "marketing_start_date": "20040901"}], "brand_name": "Allopurinol sodium", "product_id": "0143-9533_5f7a1da9-2b25-46d2-8b6b-fdb44a4e1fd7", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "0143-9533", "generic_name": "Allopurinol sodium", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Allopurinol sodium", "active_ingredients": [{"name": "ALLOPURINOL SODIUM", "strength": "500 mg/25mL"}], "application_number": "ANDA076870", "marketing_category": "ANDA", "marketing_start_date": "20040901", "listing_expiration_date": "20261231"}