aloprim

Generic: allopurinol

Labeler: mylan institutional llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name aloprim
Generic Name allopurinol
Labeler mylan institutional llc
Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
INTRAVENOUS
Active Ingredients

allopurinol sodium 500 mg/25mL

Manufacturer
Mylan Institutional LLC

Identifiers & Regulatory

Product NDC 67457-187
Product ID 67457-187_35f241ea-eeb8-41b3-9596-be40eb9af06d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA020298
Listing Expiration 2026-12-31
Marketing Start 2007-05-15

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 67457187
Hyphenated Format 67457-187

Supplemental Identifiers

RxCUI
252931 261265
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 aloprim (source: ndc)
Generic Name allopurinol (source: ndc)
Application Number NDA020298 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 500 mg/25mL
source: ndc
Packaging
  • 1 VIAL, GLASS in 1 CARTON (67457-187-50) / 25 mL in 1 VIAL, GLASS
source: ndc

Packages (1)

Ingredients (1)

allopurinol sodium (500 mg/25mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "35f241ea-eeb8-41b3-9596-be40eb9af06d", "openfda": {"unii": ["428673RC2Z"], "rxcui": ["252931", "261265"], "spl_set_id": ["10cc918f-aa44-415b-932d-2404695ac449"], "manufacturer_name": ["Mylan Institutional LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, GLASS in 1 CARTON (67457-187-50)  / 25 mL in 1 VIAL, GLASS", "package_ndc": "67457-187-50", "marketing_start_date": "20070515"}], "brand_name": "Aloprim", "product_id": "67457-187_35f241ea-eeb8-41b3-9596-be40eb9af06d", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "67457-187", "generic_name": "Allopurinol", "labeler_name": "Mylan Institutional LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Aloprim", "active_ingredients": [{"name": "ALLOPURINOL SODIUM", "strength": "500 mg/25mL"}], "application_number": "NDA020298", "marketing_category": "NDA", "marketing_start_date": "20070515", "listing_expiration_date": "20261231"}