Losartan Potassium And Hydrochlorothiazide Tablet, Film Coated
Product Images NDC 50090-5962

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 50090-5962). 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

Hydrochlorothiazide Structure (Hydrochlorothiazide Chemical Structure)

Chemical structure of losartan potassium, showing its molecular components including a chlorobenzene ring, sulfonamide group, and tetrazole ring. The image depicts the structural formula relevant to the active ingredient losartan potassium in the product Losartan Potassium and Hydrochlorothiazide.*

FDA Label Image

Label Image (Lbl500905962)

Losartan Potassium and Hydrochlorothiazide 50 mg/12.5 mg film coated tablets label from A-S Medication Solutions. The label displays product name, dosage strengths, package contents of 90 tablets, lot number, storage instructions to protect from light and keep at 68 to 77 degrees Fahrenheit, and directions to see package insert for dosing. The label also shows the product NDC 50090-5962-0 and distributor location in Libertyville, Illinois.*

FDA Label Image

Losartan Potassium Structure (Losartan Potassium Chemical Structure)

Chemical structure of losartan potassium, the active ingredient in the combination drug Losartan Potassium and Hydrochlorothiazide. The diagram shows the molecular framework including a tetrazole ring and potassium ion.*

* 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.