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  5. NDC Package Code: 57297-216-03 Losartan Potassium And Hydrochlorothiazide

NDC Package 57297-216-03 Losartan Potassium And Hydrochlorothiazide

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 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:
57297-216-03
Package Description:
1000 TABLET in 1 BOTTLE
Product Code:
57297-216
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:
57297021603
NDC to RxNorm Crosswalk:
  • RxCUI: 979464 - losartan potassium 100 MG / hydroCHLOROthiazide 12.5 MG Oral Tablet
  • RxCUI: 979464 - hydrochlorothiazide 12.5 MG / losartan potassium 100 MG Oral Tablet
  • RxCUI: 979464 - HCTZ 12.5 MG / Losartan K+ 100 MG Oral Tablet
  • RxCUI: 979464 - HCTZ 12.5 MG / Losartan Pot 100 MG Oral Tablet
  • RxCUI: 979464 - HCTZ 12.5 MG / losartan potassium 100 MG Oral Tablet
    • Labeler Name:
    Lupin Limited
    Sample Package:
    No
    Start Marketing Date:
    10-06-2010
    Listing Expiration Date:
    12-31-2017
    Exclude Flag:
    I
    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
    57297-216-01100 TABLET in 1 BOTTLE
    57297-216-0630 TABLET in 1 BOTTLE
    57297-216-0990 TABLET in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 57297-216-03?

    The NDC Packaged Code 57297-216-03 is assigned to a package of 1000 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 57297-216 included in the NDC Directory?

    No, Losartan Potassium And Hydrochlorothiazide with product code 57297-216 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Lupin Limited on October 06, 2010 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 57297-216-03?

    The 11-digit format is 57297021603. 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 Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-257297-216-035-4-257297-0216-03