NDC Package 63739-143-10 Tamoxifen Citrate

Tablet, Film Coated 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:
63739-143-10
Package Description:
10 BLISTER PACK in 1 BOX, UNIT-DOSE / 10 TABLET, FILM COATED in 1 BLISTER PACK
Product Code:
Proprietary Name:
Tamoxifen Citrate
Non-Proprietary Name:
Tamoxifen Citrate
Substance Name:
Tamoxifen Citrate
Usage Information:
Tamoxifen is used to treat breast cancer. It is also used to reduce the chances of breast cancer in high-risk patients. This medication can block the growth of breast cancer. It works by interfering with the effects of estrogen in the breast tissue.
11-Digit NDC Billing Format:
63739014310
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
10 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 198240 - tamoxifen citrate 10 MG Oral Tablet
  • RxCUI: 198240 - tamoxifen 10 MG Oral Tablet
  • RxCUI: 198240 - tamoxifen 10 MG (as tamoxifen citrate 15.2 MG) Oral Tablet
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Mckesson Corporation Dba Sky Packaging
    Dosage Form:
    Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA075797
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    12-14-2021
    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 63739-143-10?

    The NDC Packaged Code 63739-143-10 is assigned to a package of 10 blister pack in 1 box, unit-dose / 10 tablet, film coated in 1 blister pack of Tamoxifen Citrate, a human prescription drug labeled by Mckesson Corporation Dba Sky Packaging. The product's dosage form is tablet, film coated and is administered via oral form.

    Is NDC 63739-143 included in the NDC Directory?

    Yes, Tamoxifen Citrate with product code 63739-143 is active and included in the NDC Directory. The product was first marketed by Mckesson Corporation Dba Sky Packaging on December 14, 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 NDC billing unit for package 63739-143-10?

    The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 10.

    What is the 11-digit format for NDC 63739-143-10?

    The 11-digit format is 63739014310. 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
    5-3-263739-143-105-4-263739-0143-10