NDC Package 65862-074-24 Citalopram Hydrobromide

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:
65862-074-24
Package Description:
240 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Citalopram Hydrobromide
Non-Proprietary Name:
Citalopram Hydrobromide
Substance Name:
Citalopram Hydrobromide
Usage Information:
Citalopram is used to treat depression. It may improve your energy level and feelings of well-being. Citalopram is known as a selective serotonin reuptake inhibitor (SSRI). This medication works by helping to restore the balance of a certain natural substance (serotonin) in the brain.
11-Digit NDC Billing Format:
65862007424
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
240 ML
NDC to RxNorm Crosswalk:
  • RxCUI: 309313 - citalopram 10 MG in 5 mL Oral Solution
  • RxCUI: 309313 - citalopram 2 MG/ML Oral Solution
  • RxCUI: 309313 - citalopram (as citalopram hydrobromide) 2 MG/ML Oral Solution
  • RxCUI: 309313 - citalopram 10 MG per 5 ML Oral Solution
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Aurobindo Pharma Limited
    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:
    ANDA077812
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    08-28-2006
    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.

    Frequently Asked Questions

    What is NDC 65862-074-24?

    The NDC Packaged Code 65862-074-24 is assigned to a package of 240 ml in 1 bottle of Citalopram Hydrobromide, a human prescription drug labeled by Aurobindo Pharma Limited. The product's dosage form is solution and is administered via oral form.

    Is NDC 65862-074 included in the NDC Directory?

    Yes, Citalopram Hydrobromide with product code 65862-074 is active and included in the NDC Directory. The product was first marketed by Aurobindo Pharma Limited on August 28, 2006 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 NDC billing unit for package 65862-074-24?

    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 240.

    What is the 11-digit format for NDC 65862-074-24?

    The 11-digit format is 65862007424. 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
    5-3-265862-074-245-4-265862-0074-24