Amlodipine Besylate
Product Images NDC 68071-1348

4 FDA label images from Nucare Pharmaceuticals,inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Amlodipine Besylate (NDC 68071-1348). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Nucare 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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Chemical structure of the active ingredient in AMLODIPINE BESYLATE by NuCare Pharmaceuticals, Inc. The diagram shows the molecular structure including rings, bonds, and functional groups, with a molecular formula notation C6H6O3S visible, representing part of the compound's chemical composition.*
FDA Label Image

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A Kaplan-Meier curve comparing event rates over 24 months between Amlodipine and placebo groups. The graph shows lower event rates for the Amlodipine group. Included are statistical values: a p-value of 0.003, hazard ratio of 0.691, and 95% confidence interval ranging from 0.54 to 0.88. The x-axis represents time in months, and the y-axis represents the event rate, with the number of subjects at risk indicated along the timeline.*
FDA Label Image

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A hazard ratio forest plot showing comparison results between amlodipine and placebo across various patient subgroups, including overall population, age, gender, baseline sitting systolic blood pressure, baseline vessel disease, vessel stenosis status, and PCI-stent strata. The horizontal axis represents hazard ratio with 95% confidence interval, indicating relative outcomes favoring either amlodipine or placebo.*
FDA Label Image

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Packaging label for Amlodipine Besylate 5 mg tablets by NuCare Pharmaceuticals, Inc. The label indicates a quantity of 90 tablets, with the product marked as Rx Only. It shows NDC 68071-1348-9 and includes manufacturer information noting Cipla Ltd., Verna Goa, India. Additional barcode and storage instructions are visible along with warnings to keep out of reach of children.*

* 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.