Amlodipine Besylate Tablet
Product Images NDC 71610-802

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Amlodipine Besylate (NDC 71610-802). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aphena Pharma Solutions - Tennessee, 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

71610-802-60 (71610 802 60)

Amlodipine Besylate USP 2.5 mg tablet bottle label displaying 90 tablets. The label includes storage instructions, manufacturer information including Oxford Pharmaceutical LLC and Aphena Pharma, batch and expiration details, NDC 71610-802-60, and denotes prescription only status (RX ONLY).*

FDA Label Image

Aphena (Aphena)

FDA Label Image

Figure-1 (Figure1)

A Kaplan-Meier survival curve showing event rates over time (months) comparing Amlodipine versus placebo. The graph includes a p-value, hazard ratio, and 95% confidence interval. The x-axis represents time in months, and the y-axis represents event rate. Numbers at risk are displayed below the x-axis at various time points.*

FDA Label Image

Figure-2 (Figure2)

A forest plot showing hazard ratios with 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 strata. The x-axis represents hazard ratios from 0.0 to 2.0, indicating effect favoring Amlodipine or placebo.*

FDA Label Image

Structure (Structure)

Chemical structure of amlodipine besylate showing its molecular components and bonding, including a chlorophenyl group, ester and amine functional groups, and a sulfonate moiety.*

* 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.