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  5. NDC Package Code: 0363-2141-01 Childrens Fexofenadine Hydrochloride Allergy

NDC Package 0363-2141-01 Childrens Fexofenadine Hydrochloride Allergy

Fexofenadine Hydrochloride Suspension 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:
0363-2141-01
Package Description:
1 BOTTLE in 1 CARTON / 240 mL in 1 BOTTLE
Product Code:
0363-2141
Proprietary Name:
Childrens Fexofenadine Hydrochloride Allergy
Non-Proprietary Name:
Fexofenadine Hydrochloride
Substance Name:
Fexofenadine Hydrochloride
Usage Information:
Shake well before usinguse only with enclosed dosing cupNote: mL = millilitersadults and children 12 years of age and overtake 10 mL every 12 hours; do not take more than 20 mL in 24 hourschildren 2 to under 12 years of agetake 5 mL every 12 hours; do not take more than 10 mL in 24 hourschildren under 2 years of ageask a doctoradults 65 years of age and olderask a doctorconsumers with kidney diseaseask a doctor
11-Digit NDC Billing Format:
00363214101
NDC to RxNorm Crosswalk:
Product Type:
Human Otc Drug
Labeler Name:
Walgreens Company
Dosage Form:
Suspension - A liquid1 dosage form that contains solid particles dispersed in a liquid vehicle.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Active Ingredient(s):
FEXOFENADINE HYDROCHLORIDE 30 mg/5mL
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
ANDA208123
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
12-06-2024
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
0363-2141-081 BOTTLE in 1 CARTON / 120 mL in 1 BOTTLE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 0363-2141-01?

The NDC Packaged Code 0363-2141-01 is assigned to a package of 1 bottle in 1 carton / 240 ml in 1 bottle of Childrens Fexofenadine Hydrochloride Allergy, a human over the counter drug labeled by Walgreens Company. The product's dosage form is suspension and is administered via oral form.

Is NDC 0363-2141 included in the NDC Directory?

Yes, Childrens Fexofenadine Hydrochloride Allergy with product code 0363-2141 is active and included in the NDC Directory. The product was first marketed by Walgreens Company on December 06, 2024 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 0363-2141-01?

The 11-digit format is 00363214101. 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 4-4-2 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
4-4-20363-2141-015-4-200363-2141-01