NDC Package 44946-1015-6 Ludent

View Billable Units, 11-Digit Format, RxNorm

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:
44946-1015-6
Package Description:
30 TABLET, CHEWABLE in 1 BLISTER PACK
Product Code:
Proprietary Name:
Ludent
Usage Information:
For once daily self-applied systemic use as a dental caries preventive in pediatric patients. It has been established that ingestion of fluoridated drinking water (1 ppm F¯) during the period of tooth development results in a significant decrease in the incidence of dental caries. Sodium Fluoride Chewable Tablets were developed to provide systemic fluoride for use as a supplement in pediatric patients from age 3 years to age 16 years and older living in areas where the drinking water fluoride contents does not exceed 0.6 ppm F¯.
11-Digit NDC Billing Format:
44946101506
NDC to RxNorm Crosswalk:
  • RxCUI: 198215 - fluoride 0.25 MG Chewable Tablet
  • RxCUI: 198215 - sodium fluoride 0.55 MG Chewable Tablet
  • RxCUI: 198215 - sodium fluoride 0.55 MG (fluoride ion 0.25 MG) Chewable Tablet
  • RxCUI: 313036 - sodium fluoride 1.1 MG Chewable Tablet
  • RxCUI: 313036 - sodium fluoride 1.1 MG (fluoride ion 0.5 MG) Chewable Tablet
  • Labeler Name:
    Sancilio & Company Inc
    Sample Package:
    No
    Start Marketing Date:
    09-10-2009
    Listing Expiration Date:
    12-31-2017
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    44946-1015-260 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC
    44946-1015-3120 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 44946-1015-6?

    The NDC Packaged Code 44946-1015-6 is assigned to a package of 30 tablet, chewable in 1 blister pack of Ludent, labeled by Sancilio & Company Inc. The product's dosage form is and is administered via form.

    Is NDC 44946-1015 included in the NDC Directory?

    No, Ludent with product code 44946-1015 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Sancilio & Company Inc on September 10, 2009 and its listing in the NDC Directory is set to expire on December 31, 2017 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 44946-1015-6?

    The 11-digit format is 44946101506. 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
    5-4-144946-1015-65-4-244946-1015-06