NDC Package 57297-217-06 Losartan Potassium And Hydrochlorothiazide

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:

57297-217-06

Package Description:

30 TABLET in 1 BOTTLE

Product Code:

57297-217

Proprietary Name:

Losartan Potassium And Hydrochlorothiazide

Usage Information:

Losartan and hydrochlorothiazide is contraindicated in patients who are hypersensitive to any component of this product. Because of the hydrochlorothiazide component, this product is contraindicated in patients with anuria or hypersensitivity to other sulfonamide-derived drugs.Do not co-administer aliskiren with losartan potassium and hydrochlorothiazide tablets in patients with diabetes.

11-Digit NDC Billing Format:

57297021706

Labeler Name:

Lupin Limited

Sample Package:

FDA Application Number:

ANDA078245

Marketing Category:

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

Start Marketing Date:

10-06-2010

End Marketing Date:

04-30-2013

Listing Expiration Date:

04-30-2013

Exclude Flag:

Code Structure:

57297 - Lupin Limited
- 57297-217 - Losartan Potassium And Hydrochlorothiazide
  - 57297-217-06 - 30 TABLET 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
57297-217-01	100 TABLET in 1 BOTTLE
57297-217-03	1000 TABLET in 1 BOTTLE
57297-217-09	90 TABLET in 1 BOTTLE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 57297-217-06?

The NDC Packaged Code 57297-217-06 is assigned to a package of 30 tablet in 1 bottle of Losartan Potassium And Hydrochlorothiazide, labeled by Lupin Limited. The product's dosage form is and is administered via form.

Is NDC 57297-217 included in the NDC Directory?

No, Losartan Potassium And Hydrochlorothiazide with product code 57297-217 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Lupin Limited on October 06, 2010 and its listing in the NDC Directory is set to expire on April 30, 2013 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 57297-217-06?

The 11-digit format is 57297021706. 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	57297-217-06	5-4-2	57297-0217-06

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