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  5. NDC Package Code: 70934-882-90 Allopurinol

NDC Package 70934-882-90 Allopurinol

Tablet Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
70934-882-90
Package Description:
90 TABLET in 1 BOTTLE, PLASTIC
Product Code:
70934-882
Proprietary Name:
Allopurinol
Non-Proprietary Name:
Allopurinol
Substance Name:
Allopurinol
Usage Information:
Allopurinol is used to treat gout and certain types of kidney stones. It is also used to prevent increased uric acid levels in patients receiving cancer chemotherapy. These patients can have increased uric acid levels due to release of uric acid from the dying cancer cells. Allopurinol works by reducing the amount of uric acid made by the body. Increased uric acid levels can cause gout and kidney problems.
11-Digit NDC Billing Format:
70934088290
NDC to RxNorm Crosswalk:
  • RxCUI: 197319 - allopurinol 100 MG Oral Tablet
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Denton Pharma, Inc. Dba Northwind Pharmaceuticals
    Dosage Form:
    Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • ALLOPURINOL 100 mg/1
    • Pharmacologic Class(es):
  • Xanthine Oxidase Inhibitor - [EPC] (Established Pharmacologic Class)
  • Xanthine Oxidase Inhibitors - [MoA] (Mechanism of Action)
    • Sample Package:
    No
    FDA Application Number:
    ANDA071586
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    08-10-2021
    End Marketing Date:
    01-31-2025
    Exclude Flag:
    N
    Code Structure:

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    70934-882-3030 TABLET in 1 BOTTLE, PLASTIC

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 70934-882-90?

    The NDC Packaged Code 70934-882-90 is assigned to a package of 90 tablet in 1 bottle, plastic of Allopurinol, a human prescription drug labeled by Denton Pharma, Inc. Dba Northwind Pharmaceuticals. The product's dosage form is tablet and is administered via oral form.

    Is NDC 70934-882 included in the NDC Directory?

    Yes, Allopurinol with product code 70934-882 is active and included in the NDC Directory. The product was first marketed by Denton Pharma, Inc. Dba Northwind Pharmaceuticals on August 10, 2021.

    What is the 11-digit format for NDC 70934-882-90?

    The 11-digit format is 70934088290. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-270934-882-905-4-270934-0882-90