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  5. NDC Package Code: 10267-3579-6 Cetirizine Hydrochloride 10 Mg

NDC Package 10267-3579-6 Cetirizine Hydrochloride 10 Mg

Tablet, Film Coated Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

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:
10267-3579-6
Package Description:
365 TABLET, FILM COATED in 1 BOTTLE
Product Code:
10267-3579
Proprietary Name:
Cetirizine Hydrochloride 10 Mg
Non-Proprietary Name:
Cetirizine Hydrochloride 10 Mg
Substance Name:
Cetirizine Hydrochloride
Usage Information:
Adults and children 6 years and overone 10 mg tablet once daily; do not take more than one 10 mg tablet in 24 hours. A 5 mg product may be appropriate for less severe symptoms.Adults 65 years and overask a doctor Children under 6 years of ageask a doctor Consumers with liver or kidney diseaseask a doctor
11-Digit NDC Billing Format:
10267357906
NDC to RxNorm Crosswalk:
Product Type:
Human Otc Drug
Labeler Name:
Contract Pharmacal Corp.
Dosage Form:
Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Active Ingredient(s):
CETIRIZINE HYDROCHLORIDE 10 mg/1
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
ANDA076047
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
04-16-2025
Listing Expiration Date:
12-31-2026
Exclude Flag:
N
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
10267-3579-4100 TABLET, FILM COATED in 1 BOTTLE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 10267-3579-6?

The NDC Packaged Code 10267-3579-6 is assigned to a package of 365 tablet, film coated in 1 bottle of Cetirizine Hydrochloride 10 Mg, a human over the counter drug labeled by Contract Pharmacal Corp.. The product's dosage form is tablet, film coated and is administered via oral form.

Is NDC 10267-3579 included in the NDC Directory?

Yes, Cetirizine Hydrochloride 10 Mg with product code 10267-3579 is active and included in the NDC Directory. The product was first marketed by Contract Pharmacal Corp. on April 16, 2025 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 10267-3579-6?

The 11-digit format is 10267357906. 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
5-4-110267-3579-65-4-210267-3579-06