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  5. NDC Package Code: 17856-0551-1 Escitalopram Oxalate

NDC Package 17856-0551-1 Escitalopram Oxalate

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:
17856-0551-1
Package Description:
72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE / 5 mL in 1 CUP, UNIT-DOSE
Product Code:
17856-0551
Proprietary Name:
Escitalopram Oxalate
Usage Information:
Escitalopram is used to treat depression and anxiety. It works by helping to restore the balance of a certain natural substance (serotonin) in the brain. Escitalopram belongs to a class of drugs known as selective serotonin reuptake inhibitors (SSRI). It may improve your energy level and feelings of well-being and decrease nervousness.
11-Digit NDC Billing Format:
17856055101
NDC to RxNorm Crosswalk:
  • RxCUI: 351285 - escitalopram 5 MG in 5 mL Oral Solution
  • RxCUI: 351285 - escitalopram 1 MG/ML Oral Solution
  • RxCUI: 351285 - escitalopram (as escitalopram oxalate) 10 MG per 10 ML Oral Solution
  • RxCUI: 351285 - escitalopram (as escitalopram oxalate) 5 MG per 5 ML Oral Solution
    • Labeler Name:
    Atlantic Biologicals Corp
    Sample Package:
    No
    Start Marketing Date:
    05-30-2013
    Listing Expiration Date:
    12-31-2022
    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 17856-0551-1?

    The NDC Packaged Code 17856-0551-1 is assigned to a package of 72 cup, unit-dose in 1 box, unit-dose / 5 ml in 1 cup, unit-dose of Escitalopram Oxalate, labeled by Atlantic Biologicals Corp. The product's dosage form is and is administered via form.

    Is NDC 17856-0551 included in the NDC Directory?

    No, Escitalopram Oxalate with product code 17856-0551 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Atlantic Biologicals Corp on May 30, 2013 and its listing in the NDC Directory is set to expire on December 31, 2022 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 17856-0551-1?

    The 11-digit format is 17856055101. 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
    5-4-117856-0551-15-4-217856-0551-01