NDC Package 69117-0044-1 Lamotrigine

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:
69117-0044-1
Package Description:
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
Product Code:
Proprietary Name:
Lamotrigine
Usage Information:
Lamotrigine is used alone or with other medications to prevent and control seizures. It may also be used to help prevent the extreme mood swings of bipolar disorder in adults. Lamotrigine is known as an anticonvulsant or antiepileptic drug. It is thought to work by restoring the balance of certain natural substances in the brain. This drug is not approved for use in children younger than 2 years due to an increased risk of side effects (such as infections).
11-Digit NDC Billing Format:
69117004401
NDC to RxNorm Crosswalk:
  • RxCUI: 1098608 - lamoTRIgine 300 MG 24HR Extended Release Oral Tablet
  • RxCUI: 1098608 - 24 HR lamotrigine 300 MG Extended Release Oral Tablet
  • RxCUI: 1098608 - lamotrigine 300 MG 24 HR Extended Release Oral Tablet
  • RxCUI: 1146690 - lamoTRIgine 250 MG 24HR Extended Release Oral Tablet
  • RxCUI: 1146690 - 24 HR lamotrigine 250 MG Extended Release Oral Tablet
  • Labeler Name:
    Yiling Pharmaceutical, Inc.
    Sample Package:
    No
    Start Marketing Date:
    12-09-2021
    Listing Expiration Date:
    12-31-2023
    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
    69117-0044-2100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
    69117-0044-3500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 69117-0044-1?

    The NDC Packaged Code 69117-0044-1 is assigned to a package of 30 tablet, film coated, extended release in 1 bottle of Lamotrigine, labeled by Yiling Pharmaceutical, Inc.. The product's dosage form is and is administered via form.

    Is NDC 69117-0044 included in the NDC Directory?

    No, Lamotrigine with product code 69117-0044 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Yiling Pharmaceutical, Inc. on December 09, 2021 and its listing in the NDC Directory is set to expire on December 31, 2023 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 69117-0044-1?

    The 11-digit format is 69117004401. 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
    5-4-169117-0044-15-4-269117-0044-01