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  5. NDC Package Code: 67046-355-30 Escitalopram

NDC Package 67046-355-30 Escitalopram

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:
67046-355-30
Package Description:
30 TABLET, FILM COATED in 1 BLISTER PACK
Product Code:
67046-355
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:
67046035530
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
    • Labeler Name:
    Contract Pharmacy Services-pa
    Sample Package:
    No
    Start Marketing Date:
    06-15-2020
    Listing Expiration Date:
    12-31-2021
    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 67046-355-30?

    The NDC Packaged Code 67046-355-30 is assigned to a package of 30 tablet, film coated in 1 blister pack of Escitalopram, labeled by Contract Pharmacy Services-pa. The product's dosage form is and is administered via form.

    Is NDC 67046-355 included in the NDC Directory?

    No, Escitalopram with product code 67046-355 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Contract Pharmacy Services-pa on June 15, 2020 and its listing in the NDC Directory is set to expire on December 31, 2021 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 67046-355-30?

    The 11-digit format is 67046035530. 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
    5-3-267046-355-305-4-267046-0355-30