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Tramadol Hydrochloride Tablet, Film Coated
Product Images NDC 29300-355
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Tramadol Hydrochloride (NDC 29300-355). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Unichem Pharmaceuticals (usa), 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.
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Chemical structure of Tramadol Hydrochloride shown as a molecular diagram with a cyclohexane ring, a phenyl ring with a methoxy group, and an amine with two methyl groups, associated with hydrochloride (HCl).*
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A pharmacokinetic plot showing concentration (ng/mL) versus time (hours) for Tramadol and its metabolite M1. The graph compares multiple dose and single dose concentrations over a 48-hour period, with Tramadol showing higher concentrations than M1 and multiple doses exceeding single doses.*
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A line graph titled 'Protocol CAPSS-047' showing time to discontinuation due to nausea or vomiting during a double-blind study. The x-axis represents days in the double-blind phase (0 to 25 days), and the y-axis shows percent discontinuation (0 to 50%). Two lines compare discontinuation rates: a solid red line for 10 days to 200 mg/day and a dashed blue line for 16 days to 200 mg/day, indicating higher discontinuation rates with the 10-day dosing schedule.*
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Label for Tramadol Hydrochloride 50 mg film-coated tablets by Unichem Pharmaceuticals (USA), Inc. The label displays the NDC 29300-355-01, states the product is for oral use, contains 100 tablets, and includes storage instructions at 20° to 25°C. It is marked as Rx only and manufactured by Unichem Laboratories Ltd, India.*
* 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.
