Losartan Potassium And Hydrochlorothiazide Tablet, Film Coated
Product Images NDC 42708-193

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 42708-193). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Qpharma, 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

Label (42708 193 30 Label)

Label for Losartan Potassium and Hydrochlorothiazide Tablets USP 50 mg / 12.5 mg film-coated tablets, containing 30 tablets per container. The label includes instructions for dosage and timing, the labeler QPharma, Inc., and storage directions to keep at controlled room temperature. It also states the product is Rx only and provides barcode and lot/expiration information.*

FDA Label Image

Figure-01 (73c71ed3 Figure 01)

Chemical structure of losartan potassium, showing its molecular arrangement including ketone, chloride, and potassium ions.*

FDA Label Image

Figure-02 (73c71ed3 Figure 02)

Chemical structure of losartan potassium, depicting its molecular arrangement including sulfonamide, chlorobenzene, and tetrazole ring groups.*

* 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.