NDC Package 31722-250-05 Escitalopram

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:
31722-250-05
Package Description:
500 TABLET in 1 BOTTLE
Product Code:
Proprietary Name:
Escitalopram
Usage Information:
Escitalopram is indicated for the acute and maintenance treatment of major depressive disorder in adults and in adolescents 12 to 17 years of age [see Clinical Studies (14.1)].A major depressive episode (DSM-IV) implies a prominent and relatively persistent (nearly every day for at least 2 weeks) depressed or dysphoric mood that usually interferes with daily functioning and includes at least five of the following nine symptoms: depressed mood, loss of interest in usual activities, significant change in weight and/or appetite, insomnia or hypersomnia, psychomotor agitation or retardation, increased fatigue, feelings of guilt or worthlessness, slowed thinking or impaired concentration, a suicide attempt or suicidal ideation.
11-Digit NDC Billing Format:
31722025005
NDC to RxNorm Crosswalk:
  • RxCUI: 349332 - escitalopram oxalate 10 MG Oral Tablet
  • RxCUI: 349332 - escitalopram 10 MG Oral Tablet
  • RxCUI: 349332 - escitalopram (as escitalopram oxalate) 10 MG Oral Tablet
  • RxCUI: 351249 - escitalopram oxalate 5 MG Oral Tablet
  • RxCUI: 351249 - escitalopram 5 MG Oral Tablet
  • Labeler Name:
    Camber Pharmaceuticals
    Sample Package:
    No
    Start Marketing Date:
    09-11-2012
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    31722-250-01100 TABLET in 1 BOTTLE
    31722-250-101000 TABLET in 1 BOTTLE
    31722-250-3030 TABLET in 1 BOTTLE
    31722-250-9090 TABLET in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 31722-250-05?

    The NDC Packaged Code 31722-250-05 is assigned to a package of 500 tablet in 1 bottle of Escitalopram, labeled by Camber Pharmaceuticals. The product's dosage form is and is administered via form.

    Is NDC 31722-250 included in the NDC Directory?

    No, Escitalopram with product code 31722-250 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Camber Pharmaceuticals on September 11, 2012 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 31722-250-05?

    The 11-digit format is 31722025005. 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
    5-3-231722-250-055-4-231722-0250-05