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

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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)

FDA Label Image

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

FDA Label Image

Label (Lbl713352127)

Label (Lbl713352127)
This appears to be a label of a medication called Losartan Pot., which comes in a yellow capsule with the markings HH:211. It contains a combination of Losartan and hydrochlorothiazide, and each tablet has 50/12.5mg strength. It is manufactured by Zhejiang Huahai Pharmaceutical Co. and is comparable to Hyzaar. It should be stored tightly closed at room temperature between 20°-25°C (68°_77°F). The label includes an expiration date of MM/YY and a National Drug Code of 7133521271 05032901523487.*

* 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.