Tramadol Hydrochloride
Product Images NDC 50436-0377

4 FDA label images from Unit Dose Services · 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 50436-0377). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Unit Dose Services, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Structure (Tramadol 1)

Structure (Tramadol 1)
Chemical structure of tramadol hydrochloride, showing its molecular formula with key functional groups and the hydrochloride salt component.*
FDA Label Image

Figure-1 (Tramadol 2)

Figure-1 (Tramadol 2)
A pharmacokinetic curve showing concentration (ng/mL) versus time (hours) for tramadol and its metabolite M1 after single and multiple doses. The graph includes lines for multiple dose and single dose of tramadol and M1, depicting their plasma concentration decay over 48 hours.*
FDA Label Image

Figure-2 (Tramadol 3)

Figure-2 (Tramadol 3)
A line graph titled 'Protocol CAPSS-047 Time to Discontinuation Due to Nausea/Vomiting' showing the percent of subjects discontinuing treatment over 25 days in a double-blind study with a 10-day titration to 200 mg/day dosage.*
FDA Label Image

Label Image (Lbl504360377)

Label Image (Lbl504360377)
Tramadol Hydrochloride 50 mg tablets, package contains 120 tablets. Label indicates manufacturing by Sun Pharm India Ltd, with various NDC numbers (50436-0377 and 57664-377-18). Packaging includes warnings to keep out of reach of children and storage instructions. Labeler is Unit Dose Services, LLC, Dania, FL. Product is prescription 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.