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  5. NDC Package Code: 61919-239-30 Liothyronine Sodium

NDC Package 61919-239-30 Liothyronine Sodium

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:
61919-239-30
Package Description:
30 TABLET in 1 BOTTLE
Product Code:
61919-239
Proprietary Name:
Liothyronine Sodium
Usage Information:
Liothyronine is used to treat an underactive thyroid (hypothyroidism). It replaces or provides more thyroid hormone, which is normally made by the thyroid gland. Liothyronine is a man-made form of thyroid hormone. Low thyroid hormone levels can occur naturally or when the thyroid gland is injured by radiation/medications or removed by surgery. Having enough thyroid hormone helps you stay healthy. For children, having enough thyroid hormone helps them grow and learn normally. This medication is also used to treat other types of thyroid problems (such as certain types of goiters, thyroid cancer). It can also be used to test for certain types of thyroid disease. This medication should not be used to treat infertility unless it is caused by low thyroid hormone levels.
11-Digit NDC Billing Format:
61919023930
NDC to RxNorm Crosswalk:
  • RxCUI: 903456 - liothyronine sodium 5 MCG Oral Tablet
  • RxCUI: 903456 - liothyronine sodium 0.005 MG Oral Tablet
    • Labeler Name:
    Direct Rx
    Sample Package:
    No
    Start Marketing Date:
    10-30-2017
    Listing Expiration Date:
    12-31-2022
    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 61919-239-30?

    The NDC Packaged Code 61919-239-30 is assigned to a package of 30 tablet in 1 bottle of Liothyronine Sodium, labeled by Direct Rx. The product's dosage form is and is administered via form.

    Is NDC 61919-239 included in the NDC Directory?

    No, Liothyronine Sodium with product code 61919-239 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Direct Rx on October 30, 2017 and its listing in the NDC Directory is set to expire on December 31, 2022 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 61919-239-30?

    The 11-digit format is 61919023930. 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 5-3-2 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
    5-3-261919-239-305-4-261919-0239-30