Losartan Potassium And Hydrochlorothiazide Tablet, Film Coated
Product Images NDC 42708-036

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 42708-036). 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

42708 036 30

Losartan Potassium and Hydrochlorothiazide Tablets USP, 50 mg/12.5 mg, film-coated oral tablets, 30 count. The label indicates it is a sample not for sale, includes storage instructions for controlled room temperature, and directions for dosage to be filled in. Distributed by QPharma, Inc., Cedar Knolls, NJ. The product is Rx only.*

FDA Label Image

Image 1

Chemical structure of Losartan Potassium, showing its molecular components including the biphenyl group, tetrazole ring, and potassium ion (K+).*

FDA Label Image

Image 2

Chemical structure diagram of an active ingredient, showing a sulfonamide group, chlorine atom, and a cyclic structure characteristic of a sulfonamide antibiotic or related compound. The specific molecule name is not labeled in the image.*

* 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.