Tramadol Hydrochloride
Product Images NDC 53002-4322

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 Tramadol Hydrochloride (NDC 53002-4322). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rpk Pharmaceuticals, Inc., 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 (Tramadol 1)

Structure (Tramadol 1)
Chemical structure of tramadol hydrochloride showing its molecular framework with labeled atoms and bonds.*
FDA Label Image

Figure 1 (Tramadol 2)

Figure 1 (Tramadol 2)
A line graph showing concentration (ng/mL) over time (hours) for tramadol and its metabolite M1. It compares multiple dose and single dose curves for both tramadol and M1, illustrating pharmacokinetic profiles up to 48 hours.*
FDA Label Image

Figure 2 (Tramadol 3)

Figure 2 (Tramadol 3)
A line graph depicting the time to discontinuation due to nausea and vomiting during a double-blind study titled "Protocol CAPSS-047." The x-axis shows days in double-blind treatment, ranging from 0 to 25 days. The y-axis shows the percentage of participants discontinuing, ranging from 0% to 50%. The graph traces the percent discontinuing over 10 days up to a 200 mg/day dose.*
FDA Label Image

Label Image (Lbl530024322)

Label Image (Lbl530024322)
Label for Tramadol Hydrochloride 50mg tablets by RPK Pharmaceuticals, Inc. The label indicates 20 tablets per package and includes dosing instructions to take one tablet every six hours as needed. It displays product NDC 53002-4322 and is designed for prescription use only.*

* 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.