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  5. NDC Package Code: 0722-7121-01 Chenodiol

NDC Package 0722-7121-01 Chenodiol

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:
0722-7121-01
Package Description:
1 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Product Code:
0722-7121
Proprietary Name:
Chenodiol
Usage Information:
Chenodiol is indicated for patients with radiolucent stones in well-opacifying gallbladders, in whom selective surgery would be undertaken except for the presence of increased surgical risk due to systemic disease or age. The likelihood of successful dissolution is far greater if the stones are floatable or small. For patients with nonfloatable stones, dissolution is less likely and added weight should be given to the risk that more emergent surgery might result form a delay due to unsuccessful treatment. Safety of use beyond 24 months is not established. Chenodiol will not dissolve calcified (radiopaque) or radiolucent bile pigment stones.
11-Digit NDC Billing Format:
00722712101
NDC to RxNorm Crosswalk:
  • RxCUI: 618469 - chenodiol 250 MG Oral Tablet
  • RxCUI: 618469 - chenodeoxycholate 250 MG Oral Tablet
    • Labeler Name:
    Nexgen Pharma, Inc.
    Sample Package:
    No
    Start Marketing Date:
    10-22-2009
    Listing Expiration Date:
    12-31-2020
    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 0722-7121-01?

    The NDC Packaged Code 0722-7121-01 is assigned to a package of 1 tablet, film coated in 1 bottle, plastic of Chenodiol, labeled by Nexgen Pharma, Inc.. The product's dosage form is and is administered via form.

    Is NDC 0722-7121 included in the NDC Directory?

    No, Chenodiol with product code 0722-7121 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Nexgen Pharma, Inc. on October 22, 2009 and its listing in the NDC Directory is set to expire on December 31, 2020 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 0722-7121-01?

    The 11-digit format is 00722712101. 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 4-4-2 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
    4-4-20722-7121-015-4-200722-7121-01