NDC Package 63868-964-24 Cetirizine Hydrochloride And Pseudoephedrine Hydrochloride

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:
63868-964-24
Package Description:
4 BLISTER PACK in 1 CARTON / 6 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (63868-964-73)
Product Code:
Proprietary Name:
Cetirizine Hydrochloride And Pseudoephedrine Hydrochloride
Usage Information:
Do not break or chew tablet; swallow tablet wholeadults and children 12 years and over     take 1 tablet every 12 hours; do not take more than 2 tablets in 24 hours.adults 65 years and over    ask a doctorchildren under 12 years of age    ask a doctorconsumers with liver or kidney disease    ask a doctor
11-Digit NDC Billing Format:
63868096424
NDC to RxNorm Crosswalk:
  • RxCUI: 1014571 - cetirizine HCl 5 MG / pseudoephedrine HCl 120 MG 12HR Extended Release Oral Tablet
  • RxCUI: 1014571 - 12 HR cetirizine hydrochloride 5 MG / pseudoephedrine hydrochloride 120 MG Extended Release Oral Tablet
  • RxCUI: 1014571 - cetirizine dihydrochloride 5 MG / pseudoephedrine HCl 120 MG 12 HR Extended Release Oral Tablet
  • Labeler Name:
    Chain Drug Marketing Association, Inc.
    Sample Package:
    No
    Start Marketing Date:
    03-03-2016
    Listing Expiration Date:
    12-31-2019
    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 63868-964-24?

    The NDC Packaged Code 63868-964-24 is assigned to a package of 4 blister pack in 1 carton / 6 tablet, film coated, extended release in 1 blister pack (63868-964-73) of Cetirizine Hydrochloride And Pseudoephedrine Hydrochloride, labeled by Chain Drug Marketing Association, Inc.. The product's dosage form is and is administered via form.

    Is NDC 63868-964 included in the NDC Directory?

    No, Cetirizine Hydrochloride And Pseudoephedrine Hydrochloride with product code 63868-964 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Chain Drug Marketing Association, Inc. on March 03, 2016 and its listing in the NDC Directory is set to expire on December 31, 2019 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 63868-964-24?

    The 11-digit format is 63868096424. 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
    5-3-263868-964-245-4-263868-0964-24