Tramadol Hydrochloride Tablet
Product Images NDC 82868-052

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Tramadol Hydrochloride (NDC 82868-052). 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

82868-052-30 (82868 052 30 Rev A 06 24)

Label for tramadol hydrochloride tablets, USP, 50 mg strength, containing 30 tablets per bottle. The label states prescription use only and provides storage instructions (20°-25°C). It is labeled under Northwind Health Company, LLC, with an NDC of 82868-052-30.*

FDA Label Image

Figure 1 (Tramadol 02)

A pharmacokinetic graph showing the plasma concentration of tramadol and its metabolite M1 over time (up to 48 hours) after single and multiple doses. Concentration (ng/mL) is plotted on the y-axis (logarithmic scale), and time (hours) is on the x-axis.*

FDA Label Image

Figure 2 (Tramadol 03)

A line graph titled 'Protocol CAPSS-047' showing time to discontinuation due to nausea and vomiting. The x-axis represents days in double-blind, ranging from 0 to 25, and the y-axis represents percent discontinuing from 0 to 50. Two groups are compared: 10 days to 200 mg/day (solid red line) and 16 days to 200 mg/day (blue dashed line), with the red line showing a higher percentage of discontinuation over time.*

FDA Label Image

Structure (Tramadol 1)

Chemical structure of tramadol hydrochloride, showing its molecular components including a cyclohexane ring, phenyl group with a methoxy substituent, and the hydrochloride salt indicated by HCl.*

* 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.