NDC Package 57664-181-31 Cetirizine Hydrochloride

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 inactivated by the FDA.

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:

57664-181-31

Package Description:

120 mL in 1 BOTTLE, GLASS

Product Code:

57664-181

Proprietary Name:

Cetirizine Hydrochloride

Usage Information:

Cetirizine hydrochloride syrup is contraindicated in those patients with a known hypersensitivity to it or any of its ingredients or hydroxyzine.

11-Digit NDC Billing Format:

57664018131

NDC to RxNorm Crosswalk:

RxCUI: 1014673 - cetirizine HCl 5 MG in 5 mL Oral Solution

RxCUI: 1014673 - cetirizine hydrochloride 1 MG/ML Oral Solution

RxCUI: 1014673 - cetirizine HCl 1 MG/ML Oral Syrup

RxCUI: 1014673 - cetirizine HCl 5 MG per 5 ML Oral Solution

Labeler Name:

Caraco Pharmaceutical Laboratories, Ltd.

Sample Package:

Start Marketing Date:

11-16-2009

Listing Expiration Date:

12-31-2017

Exclude Flag:

Code Structure:

57664 - Caraco Pharmaceutical Laboratories, Ltd.
- 57664-181 - Cetirizine Hydrochloride
  - 57664-181-31 - 120 mL in 1 BOTTLE, GLASS

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
57664-181-34	473 mL in 1 BOTTLE, GLASS

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 57664-181-31?

The NDC Packaged Code 57664-181-31 is assigned to a package of 120 ml in 1 bottle, glass of Cetirizine Hydrochloride, labeled by Caraco Pharmaceutical Laboratories, Ltd.. The product's dosage form is and is administered via form.

Is NDC 57664-181 included in the NDC Directory?

No, Cetirizine Hydrochloride with product code 57664-181 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Caraco Pharmaceutical Laboratories, Ltd. on November 16, 2009 and its listing in the NDC Directory is set to expire on December 31, 2017 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 57664-181-31?

The 11-digit format is 57664018131. 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	57664-181-31	5-4-2	57664-0181-31

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