NDC Package 71335-0888-3 Loratadine

View Billable Units, 11-Digit Format, RxNorm

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

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:
71335-0888-3
Package Description:
60 TABLET in 1 BOTTLE
Product Code:
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:
71335088803
Labeler Name:
Bryant Ranch Prepack
Sample Package:
No
FDA Application Number:
ANDA075209
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
01-21-2003
End Marketing Date:
04-23-2021
Listing Expiration Date:
04-23-2021
Exclude Flag:
D
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
71335-0888-120 TABLET in 1 BOTTLE
71335-0888-230 TABLET in 1 BOTTLE
71335-0888-414 TABLET in 1 BOTTLE
71335-0888-510 TABLET in 1 BOTTLE
71335-0888-690 TABLET in 1 BOTTLE
71335-0888-728 TABLET in 1 BOTTLE
71335-0888-815 TABLET in 1 BOTTLE
71335-0888-9100 TABLET in 1 BOTTLE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 71335-0888-3?

The NDC Packaged Code 71335-0888-3 is assigned to a package of 60 tablet in 1 bottle of Loratadine, labeled by Bryant Ranch Prepack. The product's dosage form is and is administered via form.

Is NDC 71335-0888 included in the NDC Directory?

No, Loratadine with product code 71335-0888 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Bryant Ranch Prepack on January 21, 2003 and its listing in the NDC Directory is set to expire on April 23, 2021 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 71335-0888-3?

The 11-digit format is 71335088803. 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
5-4-171335-0888-35-4-271335-0888-03