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  5. NDC Package Code: 0067-6070-10 Loratadine

NDC Package 0067-6070-10 Loratadine

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

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

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:
0067-6070-10
Package Description:
1 BLISTER PACK in 1 CARTON / 10 TABLET in 1 BLISTER PACK
Product Code:
0067-6070
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:
00067607010
Labeler Name:
Glaxosmithkline Consumer Healthcare Holdings (us) Llc
Sample Package:
No
FDA Application Number:
NDA021375
Marketing Category:
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date:
09-30-2004
End Marketing Date:
11-30-2014
Listing Expiration Date:
11-30-2014
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
0067-6070-303 BLISTER PACK in 1 CARTON / 30 TABLET in 1 BLISTER PACK

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 0067-6070-10?

The NDC Packaged Code 0067-6070-10 is assigned to a package of 1 blister pack in 1 carton / 10 tablet in 1 blister pack of Loratadine, labeled by Glaxosmithkline Consumer Healthcare Holdings (us) Llc. The product's dosage form is and is administered via form.

Is NDC 0067-6070 included in the NDC Directory?

No, Loratadine with product code 0067-6070 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Glaxosmithkline Consumer Healthcare Holdings (us) Llc on September 30, 2004 and its listing in the NDC Directory is set to expire on November 30, 2014 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 0067-6070-10?

The 11-digit format is 00067607010. 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
4-4-20067-6070-105-4-200067-6070-10