Losartan Potassium And Hydrochlorothiazide
Product Images NDC 66116-450

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 66116-450). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Medvantx, 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

Losartan Potassium Structure (7306dad3 30ed 47ed 9fb9 D5d9e1ec5247 01)

Chemical structure of losartan potassium, the active ingredient in Losartan Potassium and Hydrochlorothiazide by MedVantx, Inc. The diagram illustrates the molecular structure including various rings and functional groups along with a potassium ion (K+).*

FDA Label Image

Hctz Structure (7306dad3 30ed 47ed 9fb9 D5d9e1ec5247 02)

Chemical structure of the active ingredient in Losartan Potassium and Hydrochlorothiazide as shown in the image. The diagram depicts the molecular arrangement including atoms and bonds characteristic of the compound.*

FDA Label Image

Losartan Potassium Hydrochlorothiazide 50mg/12.5mg (7306dad3 30ed 47ed 9fb9 D5d9e1ec5247 03)

Losartan Potassium and Hydrochlorothiazide Tablets, 50mg/12.5mg, blister card containing 30 tablets, labeled by MedVantx, Inc. The label includes dosing instructions referencing the package insert, storage conditions at controlled room temperature (20°-25°C or 68°-77°F), and notes that the product is prescription only and not for sale. Manufacturer listed as Teva Pharmaceuticals Ltd., Jerusalem, Israel. Additional information includes a phone number for refill assistance and distributor address in San Diego, CA.*

* 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.