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  5. NDC Package Code: 68151-1008-2 Cetirizine Hydrochloride

NDC Package 68151-1008-2 Cetirizine Hydrochloride

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:
68151-1008-2
Package Description:
1 mL in 1 PACKAGE
Product Code:
68151-1008
Proprietary Name:
Cetirizine Hydrochloride
Usage Information:
Perennial Allergic Rhinitis:Cetirizine hydrochloride is indicated for the relief of symptoms associated with perennial allergic rhinitis due to allergens such as dust mites, animal dander and molds in children 6 to 23 months of age. Symptoms treated effectively include sneezing, rhinorrhea, postnasal discharge, nasal pruritus, ocular pruritus, and tearing.Chronic Urticaria:Cetirizine hydrochloride is indicated for the treatment of the uncomplicated skin manifestations of chronic idiopathic urticaria in children 6 months to 5 years of age. It significantly reduces the occurrence, severity, and duration of hives and significantly reduces pruritus.
11-Digit NDC Billing Format:
68151100802
NDC to RxNorm Crosswalk:
  • RxCUI: 1014673 - cetirizine HCl 5 MG in 5 mL Oral Solution
  • RxCUI: 1014673 - cetirizine hydrochloride 1 MG/ML Oral Solution
  • RxCUI: 1014673 - cetirizine HCl 1 MG/ML Oral Syrup
  • RxCUI: 1014673 - cetirizine HCl 5 MG per 5 ML Oral Solution
    • Labeler Name:
    Carilion Materials Management
    Sample Package:
    No
    Start Marketing Date:
    07-24-2008
    Listing Expiration Date:
    12-31-2018
    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 68151-1008-2?

    The NDC Packaged Code 68151-1008-2 is assigned to a package of 1 ml in 1 package of Cetirizine Hydrochloride, labeled by Carilion Materials Management. The product's dosage form is and is administered via form.

    Is NDC 68151-1008 included in the NDC Directory?

    No, Cetirizine Hydrochloride with product code 68151-1008 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Carilion Materials Management on July 24, 2008 and its listing in the NDC Directory is set to expire on December 31, 2018 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 68151-1008-2?

    The 11-digit format is 68151100802. 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
    5-4-168151-1008-25-4-268151-1008-02