Tramadol Hydrochloride Tablet, Film Coated
Product Images NDC 59651-441

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Tramadol Hydrochloride (NDC 59651-441). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurobindo Pharma Limited, 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

Figure1 (Tramadol Fig1)

A line graph showing concentration (ng/mL) versus time (hours) for Tramadol Hydrochloride and its metabolite M1 following single and multiple doses. Four curves represent Tramadol multiple dose, Tramadol single dose, M1 multiple dose, and M1 single dose, indicating concentration changes over a 48-hour period.*

FDA Label Image

Clinical Studies Section (Tramadol Fig2)

A line graph titled 'Protocol CAPSS-047 Time to Discontinuation Due to Nausea/Vomiting' showing percent discontinuing on the y-axis and days in double-blind on the x-axis. It compares two groups: one with 10 days to 200 mg/day and another with 16 days to 200 mg/day using stepped line and dashed line patterns, respectively.*

FDA Label Image

Tramadol-fig3 (Tramadol Fig3)

Label for traMADOL Hydrochloride Tablets USP 50 mg, film-coated tablets for further processing. The label indicates 100 tablets per container, distributed by Aurobindo Pharma USA, Inc. It includes dosage information, storage instructions, and a barcode on the right side. Manufactured in India by Aurobindo Pharma Limited.*

FDA Label Image

Structure (Tramadol Str)

Chemical structure of Tramadol Hydrochloride showing its molecular components including a methoxyphenyl group, hydroxyl group, cyclohexane ring, and dimethylamine moiety with associated hydrochloride.*

* 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.