Tramadol Hydrochloride
Product Images NDC 51138-077

View Photos of 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 51138-077). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Med-health Pharma, 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

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Chemical structure of Tramadol Hydrochloride, showing its molecular arrangement including phenyl, cyclohexanol, and dimethylamino functional groups along with the hydrochloride component.*
FDA Label Image

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A pharmacokinetic concentration versus time curve chart depicting Tramadol and its metabolite M1 in plasma. The graph compares multiple and single dose plasma concentrations over 48 hours, illustrating the concentration decay of both compounds.*
FDA Label Image

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A line plot titled 'Protocol CAPSS-047 Time to Discontinuation Due to Nausea/Vomiting' showing the percent of subjects discontinuing treatment over days in a double-blind study. The x-axis represents days (0 to 25) and the y-axis shows the percent discontinuing (0 to 50). The graph tracks discontinuation over 10 days to a 200 mg/day dose.*
FDA Label Image

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Label for Tramadol Hydrochloride Tablets 50 mg, packaged in a container of 30 tablets. The label shows the NDC 51138-077-30. Manufactured by Amneal Pharmaceuticals and repackaged by Med-Health Pharma, LLC, North Las Vegas, NV. Storage instructions specify controlled room temperature (20°-25°C). Contains caution about prescription requirement. Barcode and lot/expiration fields are visible but not filled.*

* 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.