NDC Package 25000-220-14 Cetirizine Hydrochloride Tablets, 10 Mg

Cetirizine Hydrochloride Tablet Oral - View Billable Units, 11-Digit Format, RxNorm

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:
25000-220-14
Package Description:
1000 TABLET in 1 BOTTLE
Product Code:
Proprietary Name:
Cetirizine Hydrochloride Tablets, 10 Mg
Non-Proprietary Name:
Cetirizine Hydrochloride
Substance Name:
Cetirizine Hydrochloride
Usage Information:
For 5 mg: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 tablet once a day; do not take more than 1 tablet in 24 hours.children under 6 years of ageask a doctor consumers with liver or kidney diseaseask a doctor   For 10 mg: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 doctorchildren under 6 years of ageask a doctorconsumers with liver or kidney diseaseask a doctor 
11-Digit NDC Billing Format:
25000022014
NDC to RxNorm Crosswalk:
Product Type:
Human Otc Drug
Labeler Name:
Marksans Pharma Limited
Dosage Form:
Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Sample Package:
No
FDA Application Number:
ANDA078933
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
01-13-2022
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
25000-220-031 BOTTLE in 1 CARTON / 30 TABLET in 1 BOTTLE
25000-220-081 BOTTLE in 1 CARTON / 100 TABLET in 1 BOTTLE
25000-220-781 BLISTER PACK in 1 CARTON / 7 TABLET in 1 BLISTER PACK
25000-220-811 BLISTER PACK in 1 CARTON / 14 TABLET in 1 BLISTER PACK

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 25000-220-14?

The NDC Packaged Code 25000-220-14 is assigned to a package of 1000 tablet in 1 bottle of Cetirizine Hydrochloride Tablets, 10 Mg, a human over the counter drug labeled by Marksans Pharma Limited. The product's dosage form is tablet and is administered via oral form.

Is NDC 25000-220 included in the NDC Directory?

Yes, Cetirizine Hydrochloride Tablets, 10 Mg with product code 25000-220 is active and included in the NDC Directory. The product was first marketed by Marksans Pharma Limited on January 13, 2022 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 25000-220-14?

The 11-digit format is 25000022014. 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
5-3-225000-220-145-4-225000-0220-14