NDC Package 71335-0152-6 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 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:

71335-0152-6

Package Description:

100 TABLET, FILM COATED in 1 BOTTLE

Product Code:

71335-0152

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. • In patients with anuria • For coadministration with aliskiren in patients with diabetes

11-Digit NDC Billing Format:

71335015206

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:

Bryant Ranch Prepack

Sample Package:

Start Marketing Date:

10-06-2010

Listing Expiration Date:

12-31-2023

Exclude Flag:

Code Structure:

71335 - Bryant Ranch Prepack
- 71335-0152 - Losartan Potassium And Hydrochlorothiazide
  - 71335-0152-6 - 100 TABLET, FILM COATED 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
71335-0152-1	90 TABLET, FILM COATED in 1 BOTTLE
71335-0152-2	60 TABLET, FILM COATED in 1 BOTTLE
71335-0152-3	30 TABLET, FILM COATED in 1 BOTTLE
71335-0152-4	120 TABLET, FILM COATED in 1 BOTTLE
71335-0152-5	58 TABLET, FILM COATED in 1 BOTTLE
71335-0152-7	180 TABLET, FILM COATED in 1 BOTTLE
71335-0152-8	1000 TABLET, FILM COATED in 1 BOTTLE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 71335-0152-6?

The NDC Packaged Code 71335-0152-6 is assigned to a package of 100 tablet, film coated in 1 bottle of Losartan Potassium And Hydrochlorothiazide, labeled by Bryant Ranch Prepack. The product's dosage form is and is administered via form.

Is NDC 71335-0152 included in the NDC Directory?

No, Losartan Potassium And Hydrochlorothiazide with product code 71335-0152 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Bryant Ranch Prepack on October 06, 2010 and its listing in the NDC Directory is set to expire on December 31, 2023 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 71335-0152-6?

The 11-digit format is 71335015206. 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 5-4-1 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
5-4-1	71335-0152-6	5-4-2	71335-0152-06

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