Amlodipine Besylate
Product Images NDC 68180-750

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Amlodipine Besylate (NDC 68180-750). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lupin 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 Amlodipine Besylate showing the amlodipine molecule complexed with besylate (benzenesulfonic acid) group.*

FDA Label Image

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Kaplan-Meier analysis chart compares composite clinical outcomes over 24 months for Amlodipine versus placebo. The x-axis shows time in months, and the y-axis shows event rate. Two curves are displayed: one for placebo with higher event rates and one for Amlodipine with lower event rates, indicating a hazard ratio of 0.691 and a p-value of 0.003.*

FDA Label Image

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A forest plot chart depicting hazard ratios with 95% confidence intervals comparing Amlodipine versus placebo across various patient subgroups, including overall population, age groups, gender, baseline sitting systolic blood pressure, baseline vessel disease, baseline vessels with stenosis, and PCI-stent strata. The x-axis represents hazard ratio values ranging from 0 to 2, with a vertical line at 1 indicating equal favorability between Amlodipine and placebo.*

FDA Label Image

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Label for Amlodipine Besylate Tablets USP 2.5 mg by Lupin Pharmaceuticals, Inc. The label states each tablet contains 2.5 mg amlodipine, packaged as 90 tablets. Dosage instructions advise to see prescribing info and storage at 20° to 25°C with protection from light. Manufactured by Lupin Limited, India, and labeled for Lupin Pharmaceuticals, Baltimore, MD.*

FDA Label Image

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Label for Amlodipine Besylate Tablets USP 2.5 mg by Lupin Pharmaceuticals, Inc. The label indicates the product contains 2.5 mg amlodipine per tablet, with a quantity of 90 tablets. It includes storage instructions, dosage and use direction to see prescribing information, and manufacturing details for Lupin Limited in India. The label also features the NDC 68180-719-09 and a barcode.*

FDA Label Image

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Label for Amlodipine Besylate Tablets USP 5 mg by Lupin Pharmaceuticals, Inc., containing 90 tablets. The label states each tablet contains amlodipine besylate USP equivalent to 5 mg amlodipine. Storage instructions and prescription-only status are noted. Manufactured by Lupin Limited in India and for Lupin Pharmaceuticals in the United States.*

FDA Label Image

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Amlodipine Besylate Tablets USP 5 mg label by Lupin Pharmaceuticals, Inc. The label shows the proprietary name and strength, states it contains 90 tablets, and includes manufacturer details for Lupin Pharmaceuticals, Inc. (Baltimore, MD) and Lupin Limited (India). It includes dosage and storage instructions and a barcode.*

FDA Label Image

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Amlodipine Besylate Tablets USP 10 mg tablet bottle label by Lupin Pharmaceuticals, Inc. The label includes the NDC 68180-752-09, dosage instructions to follow accompanying prescribing info, and storage conditions of 20° to 25°C. The package contains 90 tablets and is marked Rx only. Manufacturing details show Lupin Pharmaceuticals in Baltimore, MD, and Lupin Limited in Aurangabad, India.*

FDA Label Image

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Label for Amlodipine Besylate Tablets USP 10 mg by Lupin Pharmaceuticals, Inc. The label indicates each tablet contains 10 mg amlodipine equivalent, with a bottle count of 90 tablets. It includes dosage storage instructions and manufacturer information for Lupin Pharmaceuticals in the U.S. and Lupin Limited in India.*

* 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.