Amlodipine Besylate Tablet
Product Images NDC 51655-044

4 FDA label images from Northwind Health Company, Llc · 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 51655-044). 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.

Product Images & Figures Index

FDA Label Image

Structure (Structure)

Structure (Structure)
Chemical structure diagram of the active ingredient amlodipine besylate, showing its molecular components and bonds, including chlorine and an aromatic ring.*
FDA Label Image

Figure-1 (Figure 1)

Figure-1 (Figure 1)
A Kaplan-Meier survival curve graph showing event rates over time (months) comparing Amlodipine and Placebo groups. The event rate increases over 24 months, with Amlodipine group demonstrating a lower event rate than Placebo. The graph includes statistical data: P-value=0.003, Hazard Ratio=0.691, and 95% Confidence Interval (0.54, 0.88). Numbers at risk are shown for both groups at various time points.*
FDA Label Image

Figure-2 (Figure 2)

Figure-2 (Figure 2)
A hazard ratio forest plot showing comparative outcomes favoring Amlodipine or placebo across patient subgroups categorized by age, gender, baseline sitting systolic blood pressure, vessel disease, vessel stenosis, and PCI-stent strata. The x-axis represents hazard ratios with 95% confidence intervals, indicating treatment effect variability among groups.*
FDA Label Image

Label (51655 044 52 Rev A 11 23 Nhc)

Label (51655 044 52 Rev A 11 23 Nhc)
Label for Amlodipine Besylate Tablets, USP 5 mg, oral tablets in a bottle of 30 tablets from Northwind Health Company, LLC. The label includes storage instructions, prescription status, and a barcode for the product with NDC 51655-044-52.*

* 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.