Valsartan And Hydrochlorothiazide
Product Images NDC 53002-1787

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Valsartan And Hydrochlorothiazide (NDC 53002-1787). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rpk Pharmaceuticals, 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

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Four line graphs showing probabilities of achieving specific systolic and diastolic blood pressure targets at Week 8. Each graph plots probability percentages against baseline systolic or diastolic blood pressure values, comparing Valsartan and Hydrochlorothiazide combinations, Valsartan alone, Hydrochlorothiazide alone, and placebo.*

FDA Label Image

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Chemical structure of the active ingredient in Valsartan and Hydrochlorothiazide, showing the molecular arrangement with labeled functional groups and stereochemistry (S configuration).*

FDA Label Image

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Chemical structure of the active ingredient Valsartan and Hydrochlorothiazide, depicting a molecular diagram with labeled functional groups including a sulfonamide group and a chlorine atom on a benzene ring.*

FDA Label Image

Label Image (Lbl530021787)

Packaging label for Valsartan and Hydrochlorothiazide 320-12.5 mg tablets from RPK Pharmaceuticals, Inc. The label indicates a 90-tablet count with instructions to take 1 tablet daily or as directed. The NDC is 53002-1787. Spaces are provided for patient and prescribing information, including clinic name and prescriber details.*

* 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.