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  5. NDC Package Code: 69189-1107-1 Prempro

NDC Package 69189-1107-1 Prempro

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:
69189-1107-1
Package Description:
1 TABLET, SUGAR COATED in 1 DOSE PACK
Product Code:
69189-1107
Proprietary Name:
Prempro
Usage Information:
This medication contains 2 female hormones: an estrogen (such as conjugated estrogen, estradiol) and a progestin (such as medroxyprogesterone, norethindrone, norgestimate). It is used by women to help reduce symptoms of menopause (such as hot flashes, vaginal dryness). These symptoms are caused by the body making less estrogen. The progestin in this medication helps to reduce the risk of cancer of the uterus which can be caused by using estrogen. Women who have had their uterus removed do not need the progestin and therefore should not use this combination medication. If you are using this medication to treat symptoms only in and around the vagina, products applied directly inside the vagina should be considered before medications that are taken by mouth, absorbed through the skin, or injected. This medication may also be used by women after menopause to prevent bone loss (osteoporosis). However, there are other medications (such as raloxifene, bisphosphonates including alendronate) that are also effective in preventing bone loss and may be safer. These medications should be considered for use before estrogen/progestin treatment.
11-Digit NDC Billing Format:
69189110701
Labeler Name:
Avera Mckennan Hospital
Sample Package:
No
Start Marketing Date:
01-28-2016
Listing Expiration Date:
12-31-2018
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 69189-1107-1?

The NDC Packaged Code 69189-1107-1 is assigned to a package of 1 tablet, sugar coated in 1 dose pack of Prempro, labeled by Avera Mckennan Hospital. The product's dosage form is and is administered via form.

Is NDC 69189-1107 included in the NDC Directory?

No, Prempro with product code 69189-1107 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Avera Mckennan Hospital on January 28, 2016 and its listing in the NDC Directory is set to expire on December 31, 2018 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 69189-1107-1?

The 11-digit format is 69189110701. 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
5-4-169189-1107-15-4-269189-1107-01