1. Home
  2. Labeler Index
  3. Medstone Pharma Llc
  4. 71626-999
  5. NDC Package Code: 71626-999-08 Probenecid

NDC Package 71626-999-08 Probenecid

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:
71626-999-08
Package Description:
8 TABLET, FILM COATED in 1 BOTTLE
Product Code:
71626-999
Proprietary Name:
Probenecid
Usage Information:
This medication is used to prevent gout and gouty arthritis. It will not treat a sudden/severe attack of gout and may make it worse. Probenecid belongs to a class of drugs known as uricosurics. It lowers high levels of uric acid in your body by helping the kidneys to get rid of uric acid. When uric acid levels get too high, crystals can form in the joints, causing gout. Lowering uric acid levels may also help your kidneys. Probenecid may be prescribed in combination with certain antibiotics (such as penicillins). It increases the levels of antibiotic in the blood, which helps the antibiotic work better. Probenecid should not be used in children younger than 2 years.
11-Digit NDC Billing Format:
71626099908
NDC to RxNorm Crosswalk:
  • RxCUI: 198152 - probenecid 500 MG Oral Tablet
    • Labeler Name:
    Medstone Pharma Llc
    Sample Package:
    No
    Start Marketing Date:
    07-29-1976
    Listing Expiration Date:
    12-31-2022
    Exclude Flag:
    I
    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.

    Frequently Asked Questions

    What is NDC 71626-999-08?

    The NDC Packaged Code 71626-999-08 is assigned to a package of 8 tablet, film coated in 1 bottle of Probenecid, labeled by Medstone Pharma Llc. The product's dosage form is and is administered via form.

    Is NDC 71626-999 included in the NDC Directory?

    No, Probenecid with product code 71626-999 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Medstone Pharma Llc on July 29, 1976 and its listing in the NDC Directory is set to expire on December 31, 2022 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 71626-999-08?

    The 11-digit format is 71626099908. 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
    5-3-271626-999-085-4-271626-0999-08