NDC Package 51672-1348-8 Escitalopram

Escitalopram Oxalate Solution 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:
51672-1348-8
Package Description:
1 BOTTLE in 1 CARTON / 120 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Escitalopram
Non-Proprietary Name:
Escitalopram Oxalate
Substance 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:
51672134808
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
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Taro Pharmaceuticals U.s.a., Inc.
    Dosage Form:
    Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA079121
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    05-03-2012
    Listing Expiration Date:
    12-31-2024
    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
    51672-1348-11 BOTTLE in 1 CARTON / 240 mL in 1 BOTTLE
    51672-1348-91 BOTTLE in 1 CARTON / 480 mL in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 51672-1348-8?

    The NDC Packaged Code 51672-1348-8 is assigned to a package of 1 bottle in 1 carton / 120 ml in 1 bottle of Escitalopram, a human prescription drug labeled by Taro Pharmaceuticals U.s.a., Inc.. The product's dosage form is solution and is administered via oral form.

    Is NDC 51672-1348 included in the NDC Directory?

    Yes, Escitalopram with product code 51672-1348 is active and included in the NDC Directory. The product was first marketed by Taro Pharmaceuticals U.s.a., Inc. on May 03, 2012 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 51672-1348-8?

    The 11-digit format is 51672134808. 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
    5-4-151672-1348-85-4-251672-1348-08