Losartan Potassium Tablet, Film Coated
Product Images NDC 72789-044

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Losartan Potassium (NDC 72789-044). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pd-rx Pharmaceuticals, 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

72789044 Label (72789044)

This is a medication label for Losartan Potassium USP tablets in 100mg. The label indicates that the medication should be discontinued when pregnancy is detected. It advises consumers to contact a doctor for medical advice on side effects and to report adverse reactions to the FDA. The label also provides instructions on dosage and warns against tearing the label.*

FDA Label Image

Losartanfigure1 (Losartanfigure1)

FDA Label Image

Losartanfigure2 (Losartanfigure2)

This text represents a result summary of a study on the adjusted risk reduction for stroke or heart attack. The risk reduction achieved was 26% with a p-value of 0.001, indicating statistical significance. The graph shows the percentage of patients who experienced a first-line or fatal stroke or heart attack over a period of 66 months.*

FDA Label Image

Losartanfigure3 (Losartanfigure3)

FDA Label Image

Losartanfigure4 (Losartanfigure4)

This text provides information about a measure called "Risk Reduction" that seems to be represented by the number "0022". It also shows the percentage of patents with an event associated with this measure, which is 18.1%. Additionally, it mentions the time period ("Months") in which this measure was evaluated, but there is not enough context to further describe it.*

FDA Label Image

Losartanstructure (Losartanstructure)

* 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.