Losartan Potassium And Hydrochlorothiazide Tablet, Film Coated
Product Images NDC 71335-2572

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 71335-2572). 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 composition of Losartan Potassium, the active ingredient in Losartan Potassium and Hydrochlorothiazide tablets. The diagram includes atoms and bonds typical of losartan potassium's chemical format.*

FDA Label Image

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

Chemical structure of losartan potassium, showing its molecular components including a biphenyl moiety with associated functional groups.*

FDA Label Image

Label (Lbl713352572)

Label for Losartan Potassium and Hydrochlorothiazide Tablets, USP 100 mg/12.5 mg, film coated oral tablets. The label indicates 30 tablets per container, repackaged by Bryant Ranch Prepack, Inc. in Burbank, CA, and manufactured by Zhejiang Huahai Pharmaceutical Co., Ltd. Storage instructions include room temperature and light-resistant container requirements.*

* 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.