Losartan Potassium And Hydrochlorothiazide Tablet, Film Coated
Product Images NDC 72162-1700

View Photos of Packaging, Regulatory Labels, and Product Appearance

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 72162-1700). 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)

Hydrochlorothiazide Structure (Hydrochlorothiazide Chemical Structure)
Chemical structure of losartan potassium, showing its molecular composition including a chlorobenzene ring, tetrazole group, and other functional groups characteristic of this active ingredient.*
FDA Label Image

Label (Lbl721621700)

Label (Lbl721621700)
Label for Losartan Potassium and Hydrochlorothiazide Tablets USP 100 mg/12.5 mg, film-coated tablets, oral route. The label indicates a package size of 1000 tablets, relabeled by Bryant Ranch Prepack, Inc., and manufactured by Jubilant Cadista Pharmaceuticals Inc. Storage instructions and safety warnings are also included on the label.*
FDA Label Image

Losartan Potassium Structure (Losartan Potassium Chemical Structure)

Losartan Potassium Structure (Losartan Potassium Chemical Structure)
Chemical structure diagram of losartan potassium, showing the molecular arrangement and the potassium ion (K+). The diagram features detailed bonding and atoms including chlorine (Cl), nitrogen (N), and carbon (C) elements characteristic of the active ingredient losartan potassium.*

* 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.