Amlodipine Besylate Tablet
Product Images NDC 71610-722

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Amlodipine Besylate (NDC 71610-722). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aphena Pharma Solutions - Tennessee, 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

Bottle Label 5 mg (71610 0722 45)

Label for Amlodipine Besylate 5 mg oral tablets showing a package of 45 tablets. The label includes storage instructions, manufacturer information (Invagen Pharmaceuticals, Inc., and Aphena Pharma Solutions - Tennessee, LLC), NDC number 71610-0722-45, and indicates the product is RX only.*

FDA Label Image

Aphena Pharma Solutions (TN)

FDA Label Image

Fig1 (Fig1)

A line chart showing event rate over time in months comparing Amlodipine and Placebo groups. The chart includes a p-value, hazard ratio, and 95% confidence interval indicating statistical analysis results. It also lists the number of subjects at risk at various time points along the x-axis.*

FDA Label Image

Fig2 (Fig2)

A hazard ratio forest plot comparing Amlodipine besylate versus placebo across multiple patient subgroups including age, gender, baseline systolic blood pressure, baseline vessel disease, and PCI stent strata. The plot displays hazard ratios with 95% confidence intervals for each subgroup, illustrating which treatment favored outcomes based on the position relative to the line of no effect at 1.0.*

FDA Label Image

Structure (Ima)

Chemical structure of Amlodipine besylate showing its molecular arrangement with labeled functional groups and chemical bonds.*

* 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.