Losartan Potassium And Hydrochlorothiazide Tablet, Film Coated
Product Images NDC 50090-6862

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 50090-6862). 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 diagram of losartan potassium, showing its molecular composition and arrangement including a chloro-substituted biphenyl group, tetrazole ring, and sulfonamide moiety.*

FDA Label Image

Label Image (Lbl500906862)

Losartan Potassium and Hydrochlorothiazide 50 mg/12.5 mg film-coated tablets in a blister pack. The packaging label indicates each tablet contains losartan potassium USP 50 mg and hydrochlorothiazide USP 12.5 mg, with 90 tablets per pack. The labeler is A-S Medication Solutions, Libertyville, IL.*

FDA Label Image

Losartan Potassium Structure (Losartan Potassium Chemical Structure)

Chemical structure of losartan potassium, one of the active ingredients in Losartan Potassium and Hydrochlorothiazide tablets.*

* 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.