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  5. NDC Package Code: 68151-1993-0 Probenecid

NDC Package 68151-1993-0 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:
68151-1993-0
Package Description:
1 TABLET, FILM COATED in 1 PACKAGE
Product Code:
68151-1993
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:
68151199300
NDC to RxNorm Crosswalk:
  • RxCUI: 198152 - probenecid 500 MG Oral Tablet
    • Labeler Name:
    Carilion Materials Management
    Sample Package:
    No
    Start Marketing Date:
    01-13-1976
    Listing Expiration Date:
    12-31-2018
    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 68151-1993-0?

    The NDC Packaged Code 68151-1993-0 is assigned to a package of 1 tablet, film coated in 1 package of Probenecid, labeled by Carilion Materials Management. The product's dosage form is and is administered via form.

    Is NDC 68151-1993 included in the NDC Directory?

    No, Probenecid with product code 68151-1993 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Carilion Materials Management on January 13, 1976 and its listing in the NDC Directory is set to expire on December 31, 2018 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 68151-1993-0?

    The 11-digit format is 68151199300. 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 5-4-1 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
    5-4-168151-1993-05-4-268151-1993-00