NDC Package 11523-0123-1 Claritin Chewable Grape And Bubblegum

Loratadine Kit 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:
11523-0123-1
Package Description:
1 KIT in 1 CARTON
Product Code:
Proprietary Name:
Claritin Chewable Grape And Bubblegum
Non-Proprietary Name:
Loratadine
Usage Information:
This medication is an antihistamine that treats symptoms such as itching, runny nose, watery eyes, and sneezing from "hay fever" and other allergies. It is also used to relieve itching from hives. Loratadine does not prevent hives or prevent/treat a serious allergic reaction (anaphylaxis). Therefore, if your doctor has prescribed epinephrine to treat allergic reactions, always carry your epinephrine injector with you. Do not use loratadine in place of your epinephrine. If you are self-treating with this medication, it is important to read the manufacturer's package instructions carefully so you know when to consult your doctor or pharmacist. (See also Precautions section.) If you are using the tablets or capsules, do not use in children younger than 6 years unless directed by the doctor. If you are using the liquid or chewable tablets, do not use in children younger than 2 years unless directed by the doctor.
11-Digit NDC Billing Format:
11523012301
NDC to RxNorm Crosswalk:
Product Type:
Human Otc Drug
Labeler Name:
Bayer Healthcare Llc.
Dosage Form:
Kit - A packaged collection of related material.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Sample Package:
No
FDA Application Number:
NDA021891
Marketing Category:
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date:
08-23-2006
Listing Expiration Date:
12-31-2025
Exclude Flag:
N

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.

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Frequently Asked Questions

What is NDC 11523-0123-1?

The NDC Packaged Code 11523-0123-1 is assigned to a package of 1 kit in 1 carton of Claritin Chewable Grape And Bubblegum, a human over the counter drug labeled by Bayer Healthcare Llc.. The product's dosage form is kit and is administered via oral form.

Is NDC 11523-0123 included in the NDC Directory?

Yes, Claritin Chewable Grape And Bubblegum with product code 11523-0123 is active and included in the NDC Directory. The product was first marketed by Bayer Healthcare Llc. on August 23, 2006 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 11523-0123-1?

The 11-digit format is 11523012301. 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
5-4-111523-0123-15-4-211523-0123-01