Amlodipine Besylate Tablet
Product Images NDC 71335-3126

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Amlodipine Besylate (NDC 71335-3126). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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)

A forest plot chart comparing hazard ratios with 95% confidence intervals for Amlodipine versus placebo across various patient subgroups including age, gender, baseline sitting systolic blood pressure, baseline vessel disease, baseline vessels with stenosis, and PCI stent status. The x-axis shows hazard ratio values from 0.0 to 2.0, with a vertical line at 1.0 indicating equivalence between treatments.*

FDA Label Image

Figure 1 (Amlodipine Gra)

A line graph comparing event rates over time (in months) between Amlodipine and placebo groups. The y-axis shows event rates, while the x-axis shows time up to 24 months. The graph includes a p-value, hazard ratio, and 95% confidence interval, with separate curves labeled for placebo and Amlodipine, and numbers at risk indicated at the bottom.*

FDA Label Image

Amlodipine-str-2 (Amlodipine Str 2)

Chemical structure of Amlodipine besylate showing its molecular framework with annotated chemical groups and bonds.*

FDA Label Image

Label (Lbl713353126)

Label for Amlodipine Besylate Tablets, USP 2.5 mg, oral tablet form. Package contains 30 tablets. Label displays the NDC number 71335-3126-1 and identifies Bryant Ranch Prepack as the repackager and Alkem Laboratories Ltd. as the manufacturer. Includes storage instructions, QR codes for package insert and dosage information, and a barcode.*

* 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.