Amlodipine Besylate Tablet
Product Images NDC 50090-5059

4 FDA label images from A-s Medication Solutions · 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 50090-5059). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by A-s Medication Solutions, 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 chart illustrating hazard ratios and 95% confidence intervals comparing 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 horizontal axis represents hazard ratio values from 0.0 to 2.0 with a reference line at 1.0.*
FDA Label Image

Figure 1 (Amlodipine Gra)

Figure 1 (Amlodipine Gra)
A Kaplan-Meier curve showing event rate over time in months for Amlodipine versus Placebo. The graph depicts two lines representing cumulative event rates, with Amlodipine showing a lower event rate compared to Placebo over a 24-month period. The chart includes p-value, hazard ratio, and confidence interval data.*
FDA Label Image

Amlodipine-str-2 (Amlodipine Str 2)

FDA Label Image

Label Image (Lbl500905059)

Label Image (Lbl500905059)
A labeling insert for Amlodipine Besylate tablets 5 mg, oral dosage form, manufactured by A-S Medication Solutions. The label includes storage instructions to keep between 68 to 77 degrees Fahrenheit and indicates a package count of 90 tablets. It also features barcodes and manufacturing details.*

* 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.