Losartan Potassium And Hydrochlorothiazide Tablet, Film Coated
Product Images NDC 50090-7059

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 50090-7059). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by A-s Medication Solutions, 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 diagram showing the molecular arrangement of losartan potassium, an active ingredient in the drug Losartan Potassium and Hydrochlorothiazide.*

FDA Label Image

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

Chemical structure of losartan potassium, showing the molecular arrangement including a chlorinated biphenyl group, tetrazole ring, and sulfonamide functional groups.*

FDA Label Image

Label Image (Lbl500907059)

Packaging label for Losartan Potassium and Hydrochlorothiazide 100 mg/25 mg film-coated tablets by A-S Medication Solutions. The label states each tablet contains losartan potassium 100 mg and hydrochlorothiazide 25 mg. Storage instructions advise keeping at 68 to 77 degrees F and protecting from light. The package contains 90 tablets and includes dosage and packaging information, along with the product NDC 50090-7059-0.*

* 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.