NDC Package 57664-263-31 Cetirizine Hydroloride Allergy

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:
57664-263-31
Package Description:
120 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Cetirizine Hydroloride Allergy
Usage Information:
Use only with enclosed dosing cup adults and children 6 years and over1 teaspoonful (5 mL) or 2 teaspoonfuls (10 mL) once daily depending upon severity of symptoms; do not take more than 2 teaspoonfuls (10 mL) in 24 hours.adults 65 years and over1 teaspoonful (5 mL) once daily; do not take more than 1 teaspoonful (5 mL) in 24 hours.children 2 to under 6 years of age½ teaspoonful (2.5 mL) once daily.  If needed, dose can be increased to a maximum of 1 teaspoonful (5 mL) once daily or ½ teaspoonful (2.5 mL) every 12 hours. Do not give more than 1 teaspoonful (5 mL) in 24 hours.children under 2 years of ageask a doctorconsumers with liver or kidney diseaseask a doctor                              
11-Digit NDC Billing Format:
57664026331
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:
    Caraco Pharmaceutical Laboratories, Ltd
    Sample Package:
    No
    Start Marketing Date:
    12-01-2011
    Listing Expiration Date:
    12-31-2017
    Exclude Flag:
    I

    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
    57664-263-34470 mL in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 57664-263-31?

    The NDC Packaged Code 57664-263-31 is assigned to a package of 120 ml in 1 bottle of Cetirizine Hydroloride Allergy, labeled by Caraco Pharmaceutical Laboratories, Ltd. The product's dosage form is and is administered via form.

    Is NDC 57664-263 included in the NDC Directory?

    No, Cetirizine Hydroloride Allergy with product code 57664-263 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Caraco Pharmaceutical Laboratories, Ltd on December 01, 2011 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 57664-263-31?

    The 11-digit format is 57664026331. 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
    5-3-257664-263-315-4-257664-0263-31