NDC Package 69238-1276-1 Levothyroxine Sodium

Tablet Oral - View Billable Units, 11-Digit Format, RxNorm

Package Information

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:
69238-1276-1
Package Description:
100 TABLET in 1 BOTTLE
Product Code:
Proprietary Name:
Levothyroxine Sodium
Non-Proprietary Name:
Levothyroxine Sodium
Substance Name:
Levothyroxine Sodium
Usage Information:
Levothyroxine is used to treat an underactive thyroid (hypothyroidism). It replaces or provides more thyroid hormone, which is normally produced by the thyroid gland. 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 is important for maintaining normal mental and physical activity. In children, having enough thyroid hormone is important for normal mental and physical development. This medication is also used to treat other types of thyroid disorders (such as certain types of goiters, thyroid cancer). This medication should not be used to treat infertility unless it is caused by low thyroid hormone levels.
11-Digit NDC Billing Format:
69238127601
NDC to RxNorm Crosswalk:
  • RxCUI: 892246 - levothyroxine sodium 100 MCG Oral Tablet
  • RxCUI: 892246 - levothyroxine sodium 0.1 MG Oral Tablet
  • RxCUI: 892251 - levothyroxine sodium 200 MCG Oral Tablet
  • RxCUI: 892251 - levothyroxine sodium 0.2 MG Oral Tablet
  • RxCUI: 892255 - levothyroxine sodium 300 MCG Oral Tablet
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Amneal Pharmaceuticals Ny Llc
    Dosage Form:
    Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA210831
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    03-15-2021
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    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 69238-1276-1?

    The NDC Packaged Code 69238-1276-1 is assigned to a package of 100 tablet in 1 bottle of Levothyroxine Sodium, a human prescription drug labeled by Amneal Pharmaceuticals Ny Llc. The product's dosage form is tablet and is administered via oral form.

    Is NDC 69238-1276 included in the NDC Directory?

    Yes, Levothyroxine Sodium with product code 69238-1276 is active and included in the NDC Directory. The product was first marketed by Amneal Pharmaceuticals Ny Llc on March 15, 2021 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 69238-1276-1?

    The 11-digit format is 69238127601. 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
    5-4-169238-1276-15-4-269238-1276-01