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  5. NDC Package Code: 65597-115-07 Tribenzor

NDC Package 65597-115-07 Tribenzor

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 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:
65597-115-07
Package Description:
7 TABLET, FILM COATED in 1 BOTTLE
Product Code:
65597-115
Proprietary Name:
Tribenzor
Usage Information:
This product is used to treat high blood pressure (hypertension). Lowering high blood pressure helps prevent strokes, heart attacks, and kidney problems. This product contains 3 medications: olmesartan, amlodipine, and hydrochlorothiazide. Olmesartan is an angiotensin receptor blocker (ARB) and amlodipine is a calcium channel blocker. They both work by relaxing blood vessels so blood can flow more easily. Hydrochlorothiazide is called a "water pill" (diuretic) and causes your body to get rid of extra salt and water by making more urine.
11-Digit NDC Billing Format:
65597011507
Labeler Name:
Daiichi Sankyo, Inc.
Sample Package:
No
FDA Application Number:
NDA200175
Marketing Category:
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date:
07-31-2010
End Marketing Date:
07-31-2023
Listing Expiration Date:
07-31-2023
Exclude Flag:
D
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
65597-115-1010 BLISTER PACK in 1 BOX / 10 TABLET, FILM COATED in 1 BLISTER PACK
65597-115-3030 TABLET, FILM COATED in 1 BOTTLE
65597-115-707 TABLET, FILM COATED in 1 BLISTER PACK
65597-115-9090 TABLET, FILM COATED in 1 BOTTLE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 65597-115-07?

The NDC Packaged Code 65597-115-07 is assigned to a package of 7 tablet, film coated in 1 bottle of Tribenzor, labeled by Daiichi Sankyo, Inc.. The product's dosage form is and is administered via form.

Is NDC 65597-115 included in the NDC Directory?

No, Tribenzor with product code 65597-115 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Daiichi Sankyo, Inc. on July 31, 2010 and its listing in the NDC Directory is set to expire on July 31, 2023 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 65597-115-07?

The 11-digit format is 65597011507. 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
5-3-265597-115-075-4-265597-0115-07