Katerzia Suspension
Product Images NDC 52652-5001

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Katerzia (NDC 52652-5001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Azurity 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

Structural Formula (Image 01)

Chemical structure diagram of the active ingredient Amlodipine, showing its molecular configuration with labeled atoms and bonds.*

FDA Label Image

Figure 1 (Image 02)

A Kaplan-Meier survival curve chart comparing event rates over 24 months between Amlodipine and Placebo groups. The x-axis shows time in months and the y-axis shows event rate. The chart includes a p-value of 0.003, a hazard ratio of 0.691, and a 95% confidence interval from 0.54 to 0.88. Numbers at risk for each group are shown below the x-axis at multiple time points.*

FDA Label Image

Figure 2 (Image 03)

A forest plot illustrating the hazard ratios with 95% confidence intervals comparing Amlodipine and placebo across various patient subgroups including overall, age groups, gender, baseline sitting systolic blood pressure, vessel disease status, vessel stenosis, and PCI stent strata. The x-axis represents the hazard ratio scale from 0.0 to 2.0, with a vertical line indicating no effect at 1.0.*

FDA Label Image

Principal Display Panel (Bottle Label)

Label for Katerzia (amlodipine) oral suspension 1 mg/mL, 150 mL, by Azurity Pharmaceuticals, Inc. The label includes dosage strength, volume, NDC 52652-5001-1, storage instructions to refrigerate at 2°-8°C and to shake before use, and a warning 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.