Amlodipine Besylate Tablet
Product Images NDC 82868-031

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Amlodipine Besylate (NDC 82868-031). 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

Structure (14b2acb6 Ce0c 4f70 9d0a B6726c945ac2 01)

Chemical structure diagram of Amlodipine Besylate, illustrating its molecular composition including chlorine, oxygen, nitrogen atoms, and other molecular groups representative of the active ingredient in this prescription drug.*

FDA Label Image

Figure 01 (14b2acb6 Ce0c 4f70 9d0a B6726c945ac2 02)

A Kaplan-Meier curve showing the event rate over time (months) for two groups: one receiving Amlodipine and the other a placebo. The graph includes a p-value, hazard ratio, and 95% confidence interval, indicating statistical analysis of the event rates between the groups over a 24-month period.*

FDA Label Image

Figure 02 (14b2acb6 Ce0c 4f70 9d0a B6726c945ac2 03)

A forest plot illustrating hazard ratios with 95% confidence intervals for different patient subgroups comparing Amlodipine versus placebo. The subgroups include overall population, age, gender, baseline sitting systolic blood pressure, baseline vessel disease, baseline vessels with stenosis, and PCI-stent strata. The plot visually indicates whether outcomes favor Amlodipine or placebo.*

FDA Label Image

Logo (14b2acb6 Ce0c 4f70 9d0a B6726c945ac2 04)

FDA Label Image

Logo (14b2acb6 Ce0c 4f70 9d0a B6726c945ac2 05)

FDA Label Image

82868-031-90 (82868 031 90 Rev A 12 23)

Label for Amlodipine Besylate tablets, USP 10 mg, oral dosage form. The label shows a bottle containing 90 tablets, manufactured by Northwind Health Company, LLC. It includes storage instructions and a barcode, with a note indicating prescription-only status.*

* 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.