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  5. NDC Package Code: 68151-0312-1 Dipentum

NDC Package 68151-0312-1 Dipentum

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:
68151-0312-1
Package Description:
1 CAPSULE, GELATIN COATED in 1 BLISTER PACK
Product Code:
68151-0312
Proprietary Name:
Dipentum
Usage Information:
Olsalazine is used to treat a certain type of bowel disease called ulcerative colitis. It does not cure ulcerative colitis, but it may decrease symptoms such as stomach pain, diarrhea, and rectal bleeding caused by irritation/swelling of the colon/rectum. After an attack is treated, olsalazine is used to increase the amount of time between attacks. Olsalazine is a salicylate anti-inflammatory drug. It is believed to work by blocking the production of certain natural substances (e.g., prostaglandins) that may cause pain and swelling.
11-Digit NDC Billing Format:
68151031201
NDC to RxNorm Crosswalk:
  • RxCUI: 905162 - olsalazine sodium 250 MG Oral Capsule
  • RxCUI: 905164 - Dipentum 250 MG Oral Capsule
  • RxCUI: 905164 - olsalazine sodium 250 MG Oral Capsule [Dipentum]
    • Labeler Name:
    Carilion Materials Management
    Sample Package:
    No
    Start Marketing Date:
    05-15-2015
    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 68151-0312-1?

    The NDC Packaged Code 68151-0312-1 is assigned to a package of 1 capsule, gelatin coated in 1 blister pack of Dipentum, labeled by Carilion Materials Management. The product's dosage form is and is administered via form.

    Is NDC 68151-0312 included in the NDC Directory?

    No, Dipentum with product code 68151-0312 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 May 15, 2015 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 68151-0312-1?

    The 11-digit format is 68151031201. 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
    5-4-168151-0312-15-4-268151-0312-01