NDC Package 47335-175-18 Levocetirizine Dihydrochloride

View Billable Units, 11-Digit Format, RxNorm

Package Information
Other Packages
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:

47335-175-18

Package Description:

1000 TABLET, FILM COATED in 1 BOTTLE

Product Code:

47335-175

Proprietary Name:

Levocetirizine Dihydrochloride

Usage Information:

Levocetirizine is an antihistamine used to relieve allergy symptoms such as watery eyes, runny nose, itching eyes/nose, and sneezing. It is also used to relieve itching and hives. It works by blocking a certain natural substance (histamine) that your body makes during an allergic reaction. Levocetirizine does not prevent hives or prevent/treat a serious allergic reaction (such as anaphylaxis). If your doctor has prescribed epinephrine to treat allergic reactions, always carry your epinephrine injector with you. Do not use levocetirizine in place of your epinephrine.

11-Digit NDC Billing Format:

47335017518

Labeler Name:

Sun Pharma Global Fze

Sample Package:

FDA Application Number:

ANDA090362

Marketing Category:

ANDA - A product marketed under an approved Abbreviated New Drug Application.

Start Marketing Date:

02-05-2013

End Marketing Date:

10-31-2017

Listing Expiration Date:

10-31-2017

Exclude Flag:

Code Structure:

47335 - Sun Pharma Global Fze
- 47335-175 - Levocetirizine Dihydrochloride
  - 47335-175-18 - 1000 TABLET, FILM COATED in 1 BOTTLE

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 Code	Package Description
47335-175-08	100 TABLET, FILM COATED in 1 BOTTLE
47335-175-81	90 TABLET, FILM COATED in 1 BOTTLE
47335-175-83	30 TABLET, FILM COATED in 1 BOTTLE
47335-175-88	100 TABLET, FILM COATED in 1 BOTTLE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 47335-175-18?

The NDC Packaged Code 47335-175-18 is assigned to a package of 1000 tablet, film coated in 1 bottle of Levocetirizine Dihydrochloride, labeled by Sun Pharma Global Fze. The product's dosage form is and is administered via form.

Is NDC 47335-175 included in the NDC Directory?

No, Levocetirizine Dihydrochloride with product code 47335-175 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Sun Pharma Global Fze on February 05, 2013 and its listing in the NDC Directory is set to expire on October 31, 2017 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 47335-175-18?

The 11-digit format is 47335017518. 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 Format	10-Digit Original Code	11-Digit Format	11-Digit Code
5-3-2	47335-175-18	5-4-2	47335-0175-18

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