Tramadol Hydrochloride Tablet
Product Images NDC 71335-2612

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Tramadol Hydrochloride (NDC 71335-2612). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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

Label (Lbl713352612)

Label for tramadol hydrochloride tablets USP 50 mg, oral dosage form. The package contains 8 tablets packaged by Bryant Ranch Prepack, labeled as Rx only, and manufactured by Elysium Pharmaceuticals Limited. The label includes storage instructions, safety warnings, two QR codes, and barcodes.*

FDA Label Image

Figure 1 (Tramadol 02)

A line graph depicting the concentration (ng/mL) of tramadol and its metabolite M1 over time (hours). The graph compares multiple dose and single dose profiles, showing concentration decay of tramadol and M1 from 0 to 48 hours with distinct line styles for each condition.*

FDA Label Image

Figure 2 (Tramadol 03)

A line graph titled 'Protocol CAPSS-047' showing percent discontinuation due to nausea and vomiting over 25 days in a double-blind study. Two treatment groups are compared: 10 days to 200 mg/day (solid red line) and 16 days to 200 mg/day (blue dashed line). The red line shows higher cumulative discontinuation rates, reaching about 50%, while the blue line reaches around 22% by day 25.*

FDA Label Image

Structure (Tramadol 1)

Chemical structure of tramadol hydrochloride, showing its cyclohexanol ring with attached methoxyphenyl group, hydroxyl group, and dimethylaminomethyl side chain, plus the hydrochloride component.*

* 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.