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  5. NDC Package Code: 67668-161-30 Cetirizine Hydrochloride

NDC Package 67668-161-30 Cetirizine Hydrochloride

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. 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:
67668-161-30
Package Description:
30 TABLET in 1 BOTTLE
Product Code:
67668-161
Proprietary Name:
Cetirizine Hydrochloride
Usage Information:
Adults and children 6 years and over1 to 2 tablets once daily depending upon severity of symptoms; do not take more than 2 tablets in 24 hours.Adults 65 years and over1 tablet1 tablet once a day; do not take more than 1 tablet in 24 hours.Children under 6 years of ageAsk a doctorConsumers with liver or kidney diseaseAsk a doctor
11-Digit NDC Billing Format:
67668016130
NDC to RxNorm Crosswalk:
  • RxCUI: 1014676 - cetirizine HCl 5 MG Oral Tablet
  • RxCUI: 1014676 - cetirizine hydrochloride 5 MG Oral Tablet
    • Labeler Name:
    Unique Pharmaceutical Laboratories
    Sample Package:
    No
    Start Marketing Date:
    10-01-2009
    Listing Expiration Date:
    12-31-2017
    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
    67668-161-00100 TABLET in 1 BOTTLE
    67668-161-4545 TABLET in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 67668-161-30?

    The NDC Packaged Code 67668-161-30 is assigned to a package of 30 tablet in 1 bottle of Cetirizine Hydrochloride, labeled by Unique Pharmaceutical Laboratories. The product's dosage form is and is administered via form.

    Is NDC 67668-161 included in the NDC Directory?

    No, Cetirizine Hydrochloride with product code 67668-161 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Unique Pharmaceutical Laboratories on October 01, 2009 and its listing in the NDC Directory is set to expire on December 31, 2017 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 67668-161-30?

    The 11-digit format is 67668016130. 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
    5-3-267668-161-305-4-267668-0161-30