Losartan Potassium And Hydrochlorothiazide Tablet, Film Coated
Product Images NDC 71335-2127

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 71335-2127). 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

73c71ed3-figure-01 (73c71ed3 Figure 01)

Chemical structure diagram showing the molecular arrangement of the active ingredients in Losartan Potassium and Hydrochlorothiazide.*

FDA Label Image

73c71ed3-figure-02 (73c71ed3 Figure 02)

Chemical structure diagram of losartan potassium, showing its molecular arrangement including rings, chlorine, sulfonamide, and other functional groups.*

FDA Label Image

Label (Lbl713352127)

Label of Losartan Potassium and Hydrochlorothiazide 50 mg / 12.5 mg film-coated tablets by Bryant Ranch Prepack. The label includes lot number 1523487, storage instructions to keep tightly closed at 20°-25°C (68°-77°F), and notes a comparison to Hyzaar 50/12.5 mg tablet from Zhejiang Huahai Pharmaceutical Co. The package contains 90 tablets with NDC 71335-2127.*

* 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.