Tramadol Hydrochloride Tablet
Product Images NDC 60760-727

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Tramadol Hydrochloride (NDC 60760-727). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by St. Mary's Medical Park Pharmacy, 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 configuration including hydroxyl, methoxy groups, cyclohexane ring, and dimethylaminoethyl side chain.*

FDA Label Image

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A pharmacokinetic graph showing concentration (pg/mL) vs. time (hours) for Tramadol and its metabolite M1 after single and multiple doses. The graph includes four curves: Tramadol multiple dose, Tramadol single dose, M1 multiple dose, and M1 single dose over a 48-hour period.*

FDA Label Image

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A line graph from Protocol CAPSS-047 showing the percentage of discontinuation due to nausea or vomiting over 25 days of double-blind treatment. It compares two groups: one transitioning to 100 mg oxycodone for 10 days and another to 200 mg oxycodone for 10 days, with the vertical axis representing percent discontinuation and the horizontal axis representing days.*

FDA Label Image

727-30 (Tramadol 60760 727 30)

Packaging label for Tramadol Hydrochloride 50 mg tablets, USP, quantity 30, manufactured by Gravi Pharmaceuticals Pvt. Ltd., India, and packaged by St. Mary's Medical Park Pharmacy, Oro Valley, AZ. The label includes NDC 60760-727-30 and instructions to store at controlled room temperature 15°-30°C (59°-86°F). It also states 'Use as directed' and 'Rx 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.