Amlodipine Besylate
Product Images NDC 53002-2352

4 FDA label images from Rpk 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 53002-2352). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rpk 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

Figure 2 (Amlodipine Fig)

Figure 2 (Amlodipine Fig)
A forest plot depicting the hazard ratio with 95% confidence intervals comparing Amlodipine and placebo across various patient subgroups, including age, gender, baseline sitting systolic blood pressure, baseline vessel disease, vessel stenosis, and PCI stent status. The chart includes subgroup sizes and a reference mean sitting baseline SBP of 138 mm Hg indicated in a footnote.*
FDA Label Image

Figure 1 (Amlodipine Gra)

Figure 1 (Amlodipine Gra)
A Kaplan-Meier 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 hazard ratio of 0.691 with a 95% confidence interval (0.54, 0.88) and a p-value of 0.003, indicating statistical comparison details.*
FDA Label Image

Amlodipine-str-2 (Amlodipine Str 2)

Amlodipine-str-2 (Amlodipine Str 2)
Chemical structure of the active ingredient in Amlodipine Besylate, showing its molecular framework including chlorine, methyl, ethoxy, and sulfonate groups as depicted in the diagram.*
FDA Label Image

Label Image (Lbl530022352)

Label Image (Lbl530022352)
Amlodipine Besylate 2.5 mg tablets, packaged by RPK Pharmaceuticals, Inc. The label shows a bottle container with 100 tablets. Directions specify taking 1 tablet daily or as directed. The label includes prescription use information, lot number, and expiration date. Placeholders indicate where patient name and clinic information are to be added.*

* 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.