Amlodipine Besylate
Product Images NDC 58517-120

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Amlodipine Besylate (NDC 58517-120). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by New Horizon Rx Group, Llc, 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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Chemical structure diagram of amlodipine besylate showing its molecular configuration with labeled functional groups and elements.*

FDA Label Image

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A Kaplan-Meier curve chart showing event rates over time in months comparing Amlodipine and Placebo groups. The x-axis represents time in months up to 24, and the y-axis shows the event rate. The chart includes statistical information: P-value of 0.003, Hazard Ratio of 0.691, and 95% Confidence Interval from 0.54 to 0.88. The numbers at risk at different time points are noted below the x-axis.*

FDA Label Image

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A forest plot figure displaying hazard ratios with 95% confidence intervals comparing the effect of Amlodipine versus placebo across various patient subgroups, including age, gender, baseline sitting systolic blood pressure, baseline vessel disease, baseline vessels with stenosis, and PCI-stent status. The plot visually summarizes treatment impact in a clinical study context.*

FDA Label Image

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Label for Amlodipine Besylate Tablets USP, 10 mg, from New Horizon Rx Group, LLC. The package contains 30 tablets. The label includes the NDC number 58517-120-30, dosage information, and standard storage and prescription use instructions. The label indicates the product is prescription only (Rx Only).*

* 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.