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  5. NDC Package Code: 66116-450-30 Losartan Potassium And Hydrochlorothiazide

NDC Package 66116-450-30 Losartan Potassium And Hydrochlorothiazide

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. 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:
66116-450-30
Package Description:
30 TABLET, FILM COATED in 1 BOTTLE
Product Code:
66116-450
Proprietary Name:
Losartan Potassium And Hydrochlorothiazide
Usage Information:
Losartan potassium and hydrochlorothiazide tablets are 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.
11-Digit NDC Billing Format:
66116045030
NDC to RxNorm Crosswalk:
  • RxCUI: 979468 - losartan potassium 50 MG / hydroCHLOROthiazide 12.5 MG Oral Tablet
  • RxCUI: 979468 - hydrochlorothiazide 12.5 MG / losartan potassium 50 MG Oral Tablet
  • RxCUI: 979468 - HCTZ 12.5 MG / Losartan K+ 50 MG Oral Tablet
  • RxCUI: 979468 - HCTZ 12.5 MG / Losartan Pot 50 MG Oral Tablet
    • Labeler Name:
    Medvantx, Inc.
    Sample Package:
    No
    Start Marketing Date:
    12-20-2010
    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.

    Frequently Asked Questions

    What is NDC 66116-450-30?

    The NDC Packaged Code 66116-450-30 is assigned to a package of 30 tablet, film coated in 1 bottle of Losartan Potassium And Hydrochlorothiazide, labeled by Medvantx, Inc.. The product's dosage form is and is administered via form.

    Is NDC 66116-450 included in the NDC Directory?

    No, Losartan Potassium And Hydrochlorothiazide with product code 66116-450 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Medvantx, Inc. on December 20, 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 66116-450-30?

    The 11-digit format is 66116045030. 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
    5-3-266116-450-305-4-266116-0450-30