NDC Package 12634-629-79 Citalopram Hydrobromide

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:
12634-629-79
Package Description:
25 TABLET in 1 BOTTLE
Product Code:
Proprietary Name:
Citalopram Hydrobromide
Usage Information:
Citalopram HBr is indicated for the treatment of depression.The efficacy of citalopram HBr in the treatment of depression was established in 4-6 week, controlled trials of outpatients whose diagnosis corresponded most closely to the DSM-III and DSM-III-R category of major depressive disorder (see CLINICAL PHARMACOLOGY). 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.The antidepressant action of citalopram in hospitalized depressed patients has not been adequately studied.The efficacy of citalopram in maintaining an antidepressant response for up to 24 weeks following 6 to 8 weeks of acute treatment was demonstrated in two placebo-controlled trials (see CLINICAL PHARMACOLOGY). Nevertheless, the physician who elects to use citalopram for extended periods should periodically re-evaluate the long-term usefulness of the drug for the individual patient.
11-Digit NDC Billing Format:
12634062979
NDC to RxNorm Crosswalk:
  • RxCUI: 283672 - citalopram 10 MG Oral Tablet
  • RxCUI: 283672 - citalopram 10 MG (as citalopram HBr 12.49 MG) Oral Tablet
  • Labeler Name:
    Apotheca Inc.
    Sample Package:
    No
    Start Marketing Date:
    10-18-2007
    Listing Expiration Date:
    12-31-2020
    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
    12634-629-0010 TABLET in 1 BOTTLE
    12634-629-01100 TABLET in 1 BOTTLE
    12634-629-0935 TABLET in 1 BOTTLE
    12634-629-4040 TABLET in 1 BOTTLE
    12634-629-4242 TABLET in 1 BOTTLE
    12634-629-5050 TABLET in 1 BOTTLE
    12634-629-5212 TABLET in 1 BLISTER PACK
    12634-629-5414 TABLET in 1 BLISTER PACK
    12634-629-5720 TABLET in 1 BLISTER PACK
    12634-629-5930 TABLET in 1 BLISTER PACK
    12634-629-6060 TABLET in 1 BOTTLE
    12634-629-6110 TABLET in 1 BLISTER PACK
    12634-629-633 TABLET in 1 BLISTER PACK
    12634-629-666 TABLET in 1 BLISTER PACK
    12634-629-677 TABLET in 1 BLISTER PACK
    12634-629-699 TABLET in 1 BLISTER PACK
    12634-629-7130 TABLET in 1 BOTTLE
    12634-629-7424 TABLET in 1 BOTTLE
    12634-629-7828 TABLET in 1 BOTTLE
    12634-629-8020 TABLET in 1 BOTTLE
    12634-629-8121 TABLET in 1 BOTTLE
    12634-629-8212 TABLET in 1 BOTTLE
    12634-629-8515 TABLET in 1 BOTTLE
    12634-629-911 TABLET in 1 BLISTER PACK
    12634-629-944 TABLET in 1 BOTTLE
    12634-629-955 TABLET in 1 BOTTLE
    12634-629-966 TABLET in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 12634-629-79?

    The NDC Packaged Code 12634-629-79 is assigned to a package of 25 tablet in 1 bottle of Citalopram Hydrobromide, labeled by Apotheca Inc.. The product's dosage form is and is administered via form.

    Is NDC 12634-629 included in the NDC Directory?

    No, Citalopram Hydrobromide with product code 12634-629 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Apotheca Inc. on October 18, 2007 and its listing in the NDC Directory is set to expire on December 31, 2020 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 12634-629-79?

    The 11-digit format is 12634062979. 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
    5-3-212634-629-795-4-212634-0629-79