NDC Package 0046-1100-52 Premarin

Estrogens,Conjugated 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:
0046-1100-52
Package Description:
1 BLISTER PACK in 1 CARTON / 5 TABLET, FILM COATED in 1 BLISTER PACK
Product Code:
Proprietary Name:
Premarin
Non-Proprietary Name:
Estrogens, Conjugated
Substance Name:
Estrogens, Conjugated
Usage Information:
This medication is a female hormone. 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. 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. Certain estrogen products 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 treatment. Certain estrogen products may also be used by men and women to treat cancers (certain types of prostate cancer, breast cancer that has spread to other parts of the body) and by women who are not able to produce enough estrogen (for example, due to hypogonadism, primary ovarian failure).
11-Digit NDC Billing Format:
00046110052
NDC to RxNorm Crosswalk:
  • RxCUI: 150840 - PREMARIN 0.625 MG Oral Tablet
  • RxCUI: 150840 - estrogens, conjugated (USP) 0.625 MG Oral Tablet [Premarin]
  • RxCUI: 150840 - Premarin 0.625 MG Oral Tablet
  • RxCUI: 197660 - estrogens, conjugated 0.3 MG Oral Tablet
  • RxCUI: 197660 - estrogens, conjugated (USP) 0.3 MG Oral Tablet
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Wyeth Pharmaceuticals Llc, A Subsidiary Of Pfizer Inc.
    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:
    NDA004782
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    01-01-2006
    Listing Expiration Date:
    12-31-2025
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    0046-1100-81100 TABLET, FILM COATED in 1 BOTTLE
    0046-1100-911 BOTTLE in 1 CARTON / 1000 TABLET, FILM COATED in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 0046-1100-52?

    The NDC Packaged Code 0046-1100-52 is assigned to a package of 1 blister pack in 1 carton / 5 tablet, film coated in 1 blister pack of Premarin, a human prescription drug labeled by Wyeth Pharmaceuticals Llc, A Subsidiary Of Pfizer Inc.. The product's dosage form is tablet, film coated and is administered via oral form.

    Is NDC 0046-1100 included in the NDC Directory?

    Yes, Premarin with product code 0046-1100 is active and included in the NDC Directory. The product was first marketed by Wyeth Pharmaceuticals Llc, A Subsidiary Of Pfizer Inc. on January 01, 2006 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 0046-1100-52?

    The 11-digit format is 00046110052. 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 4-4-2 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
    4-4-20046-1100-525-4-200046-1100-52