Amlodipine Besylate Tablet
Product Images NDC 51655-291

View Photos of 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 51655-291). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northwind Health Company, 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

Label (51655 291 52)

Label (51655 291 52)
Packaging label for Amlodipine Besylate Tablets USP, 5 mg strength, in a bottle of 30 tablets. The label includes dosage form as oral tablets, highlights prescription use, storage instructions, and is labeled by Northwind Health Company, LLC with NDC 51655-291-52.*
FDA Label Image

Figure 2 (Amlodipine Fig)

Figure 2 (Amlodipine Fig)
A forest plot showing hazard ratios with 95% confidence intervals comparing Amlodipine versus placebo across various patient subgroups, including overall, age groups, gender, baseline sitting systolic blood pressure, baseline vessel disease, baseline vessels with stenosis, and PCI stent status. The x-axis represents hazard ratio values from 0.0 to 2.0.*
FDA Label Image

Figure 1 (Amlodipine Gra)

Figure 1 (Amlodipine Gra)
A Kaplan-Meier survival curve chart depicting event rates over 24 months comparing 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 and hazard ratio with 95% confidence interval, indicating statistical comparison between groups. Risk numbers at various time points are provided below the x-axis.*
FDA Label Image

Amlodipine-str-2 (Amlodipine Str 2)

Amlodipine-str-2 (Amlodipine Str 2)
Chemical structure diagram of amlodipine besylate, showing its molecular components and arrangement as part of the pharmaceutical labeling.*

* 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.