Losartan Potassium And Hydrochlorothiazide Tablet, Film Coated
Product Images NDC 70518-3404

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Losartan Potassium And Hydrochlorothiazide (NDC 70518-3404). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

73c71ed3-figure-01 (73c71ed3 Figure 01)

Chemical structure of losartan potassium displayed as a molecular diagram with labeled atoms and bonds, including chlorine, potassium ion, and various organic groups consistent with the losartan potassium molecule.*

FDA Label Image

73c71ed3-figure-02 (73c71ed3 Figure 02)

Chemical structure of losartan potassium, showing its molecular framework with labeled atoms and bonds as depicted in the image.*

FDA Label Image

Remedy_label (Remedy Label)

Losartan Potassium and Hydrochlorothiazide 50 mg/12.5 mg film-coated tablets, packaged in a container of 90 tablets. The label includes the NDC 70518-3404-00 and states the product is for prescription use only. It is repackaged by RemedyRepack Inc. in Indiana, PA, with storage instructions for 20-25°C (68-77°F). The manufacturer is Solco, Cranbury, NJ.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.