NDC Package 42023-112-01 Delestrogen

Estradiol Valerate Injection Intramuscular - 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:
Package Description:
Product Code:
Proprietary Name:
Non-Proprietary Name:
Estradiol Valerate
Substance Name:
Estradiol Valerate
Usage Information:
This medication is a female hormone (estrogen). 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. This medication may also be used by women who are not able to produce enough estrogen (for example, due to hypogonadism, primary ovarian failure) and by men to treat prostate cancer.
11-Digit NDC Billing Format:
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
5 ML
NDC to RxNorm Crosswalk:
  • RxCUI: 206620 - DELESTROGEN 10 MG/ML Injectable Solution
  • RxCUI: 206620 - estradiol valerate 10 MG/ML Injectable Solution [Delestrogen]
  • RxCUI: 206620 - Delestrogen 10 MG/ML Injectable Solution
  • RxCUI: 206715 - DELESTROGEN 20 MG/ML Injectable Solution
  • RxCUI: 206715 - estradiol valerate 20 MG/ML Injectable Solution [Delestrogen]
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Endo Usa, Inc.
    Dosage Form:
    Injection - A sterile preparation intended for parenteral use; five distinct classes of injections exist as defined by the USP.
    Administration Route(s):
  • Intramuscular - Administration within a muscle.
  • Active Ingredient(s):
    Sample Package:
    FDA Application Number:
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    End Marketing Date:
    Exclude Flag:
    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.

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    Frequently Asked Questions

    What is NDC 42023-112-01?

    The NDC Packaged Code 42023-112-01 is assigned to a package of 5 ml in 1 vial, multi-dose of Delestrogen, a human prescription drug labeled by Endo Usa, Inc.. The product's dosage form is injection and is administered via intramuscular form.

    Is NDC 42023-112 included in the NDC Directory?

    Yes, Delestrogen with product code 42023-112 is active and included in the NDC Directory. The product was first marketed by Endo Usa, Inc. on November 01, 2007.

    What is the NDC billing unit for package 42023-112-01?

    The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume. The calculated billable units for this package is 5.

    What is the 11-digit format for NDC 42023-112-01?

    The 11-digit format is 42023011201. 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