Losartan Potassium
Product Images NDC 75921-409

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Losartan Potassium (NDC 75921-409). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Life Line Home Care Services, 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

Losartan 50mg #30 Label (Losartan 50mg)

Losartan Potassium Life Line is a medication with a strength of 50 mg. The address of the manufacturer is 610 Madison Avenue, Tifton, GA 31784. The NDC number is 75921011430 and the manufacturing NDC number is 13888011490 with a manufacturing date of WP 02/20/4% 8194 AN.*

FDA Label Image

Structural Formula (Losartanpotassiumusp Figure 01)

FDA Label Image

Image (Losartanpotassiumusp Figure 02)

This appears to be a graph displaying the percentage of patients with a primary endpoint for two medications, atenolol and losartan potassium tablets, over the course of a 66-month study. The adjusted risk reduction for losartan over atenolol is 13%, with a p-value of 0.021. The text above the graph is not legible and contains some non-English characters.*

FDA Label Image

Image (Losartanpotassiumusp Figure 03)

This is a comparative study evaluating the effect of Atenolol and Losartan Potassium Tablets on patients with fatal/non-fatal stroke. The study reports an adjusted risk reduction of 25% for patients treated with Losartan Potassium Tablets, with a p-value of 0.001. The graph suggests that the risk reduction was observed over a period of 60 months, with measurements taken at regular intervals.*

FDA Label Image

Image (Losartanpotassiumusp Figure 04)

FDA Label Image

Image (Losartanpotassiumusp Figure 05)

* 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.