Losartan Potassium
Product Images NDC 71335-1328

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Losartan Potassium (NDC 71335-1328). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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

Fig1.jpg (Fig1)

The text appears to be a report on the results of a study comparing the effectiveness of two drugs, Atenolol and Losartan, in reducing the risk of a primary endpoint in a group of patients. The study lasted for 66 months and showed an adjusted risk reduction of 13%. The text also contains a graph with time intervals, but the data is not enough to properly interpret it.*

FDA Label Image

Fig2.jpg (Fig2)

FDA Label Image

Fig3.jpg (Fig3)

This appears to be a table showing the number of events and hazard ratios of stroke among patients taking Losartan and Atenolol, categorized by age, gender, race, ISH, Diabetes, and History of CVD. It is not possible to provide more details without the actual table.*

FDA Label Image

Fig4.jpg (Fig4)

The text appears to be a graph or chart showing the effectiveness of Losartan versus a placebo in reducing the risk of something by 16.1%. The graph includes certain figures and symbols, including 60, p=0.022, and various numbers ranging from 0 to 48. Without additional context, it is difficult to determine what the graph is specifically referring to.*

FDA Label Image

Image 01

FDA Label Image

Label Image (Lbl713351328)

This is a medication label. The medication is Losartan Potassium, 100mg, which is a green, round tablet that is used to manage high blood pressure. The tablet should be stored at room temperature and kept out of reach of children. The medicine is manufactured by West-Ward Pharmaceuticals Corp. The provided label shows information such as dosage instructions and Expiration date (EXP MM/YY). The NDC (National Drug Code) number provided is 7133513281 04383301523487.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.