NDC Package 66336-591-30 Synthroid

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:
66336-591-30
Package Description:
30 TABLET in 1 BOTTLE, PLASTIC
Product Code:
Proprietary Name:
Synthroid
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:
66336059130
NDC to RxNorm Crosswalk:
  • RxCUI: 966201 - SYNTHROID 150 MCG Oral Tablet
  • RxCUI: 966201 - levothyroxine sodium 0.15 MG Oral Tablet [Synthroid]
  • RxCUI: 966201 - Synthroid 0.15 MG Oral Tablet
  • RxCUI: 966201 - Synthroid 150 MCG Oral Tablet
  • RxCUI: 966225 - levothyroxine sodium 150 MCG Oral Tablet
  • Labeler Name:
    Dispensing Solutions, Inc.
    Sample Package:
    No
    Start Marketing Date:
    07-24-2002
    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.

    Frequently Asked Questions

    What is NDC 66336-591-30?

    The NDC Packaged Code 66336-591-30 is assigned to a package of 30 tablet in 1 bottle, plastic of Synthroid, labeled by Dispensing Solutions, Inc.. The product's dosage form is and is administered via form.

    Is NDC 66336-591 included in the NDC Directory?

    No, Synthroid with product code 66336-591 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Dispensing Solutions, Inc. on July 24, 2002 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 66336-591-30?

    The 11-digit format is 66336059130. 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
    5-3-266336-591-305-4-266336-0591-30