Losartan Potassium Tablet, Film Coated
Product Images NDC 42708-125

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Losartan Potassium (NDC 42708-125). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Qpharma, 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

Label (42708 125 30)

Label (42708 125 30)
This is a package instruction for the medication Losartan Potassium. It suggests a controlled dosage (not specified) and advises to consult the package insert for dosage information. The medication should be stored at room temperature. The remaining text is not readable ( error).*
FDA Label Image

Figure1 (Losartan Fig1)

Figure1 (Losartan Fig1)
The text mentions two drugs: Atenolol and Losartan Potassium. There is also a statistic of "Adjusted Risk Reduction: 13%" with a value of "p=" that is not complete. It also mentions different study months. However, without further context or information, it is not possible to provide a specific description or explanation.*
FDA Label Image

Figure2 (Losartan Fig2)

FDA Label Image

Figure 3 (Losartan Fig3)

FDA Label Image

Figure-4 (Losartan Fig4)

Figure-4 (Losartan Fig4)
This text represents the results of a study or trial comparing the effects of Losttan Potassium versus a placebo. The percentage of patients who experienced an event was 60% in the Losttan group, and 40% in the placebo group. The risk reduction was calculated to be 16.1%. The p-value was 0.022. Unfortunately, there is no context regarding the type of event or condition being studied.*
FDA Label Image

Chemical Structure (Losartan Str)

* 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.