Losartan Potassium And Hydrochlorothiazide Tablet, Film Coated
Product Images NDC 63629-2430

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 63629-2430). 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

Hydrochlorothiazide Structure (Hydrochlorothiazide Chemical Structure)

Chemical structure of losartan potassium, showing the molecular arrangement including benzene ring with chlorine and sulfonamide groups, and a tetrazole ring attached.*

FDA Label Image

Label (Lbl636292430)

Losartan Potassium and Hydrochlorothiazide Tablets, USP 100 mg/25 mg film-coated tablet label. The label includes the NDC 63629-2430-1 and indicates the product is manufactured by Jubilant Cadista Pharmaceuticals Inc. and relabeled by Bryant Ranch Prepack, Inc. The package contains 1000 tablets and the label features storage instructions and child safety warnings.*

FDA Label Image

Losartan Potassium Structure (Losartan Potassium Chemical Structure)

Chemical structure diagram of losartan potassium, an active ingredient in Losartan Potassium and Hydrochlorothiazide tablets. The diagram shows the molecular arrangement including a potassium ion (K+).*

* 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.