Tramadol Hydrochloride Tablet, Film Coated
Product Images NDC 60760-772

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Tramadol Hydrochloride (NDC 60760-772). 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

772-09 (Tramadol 772 09)

Label for Tramadol Hydrochloride Tablets USP 50 mg, film-coated oral tablets, with a quantity of 9 tablets. The label includes NDC 60760-772-09, RX number placeholders, batch and expiration date placeholders, and indicates manufacture by Rising Pharma Holdings, Inc., East Brunswick, NJ, with packaging by St. Mary's Medical Park Pharmacy, Oro Valley, AZ. Storage instructions specify controlled room temperature between 15°-30°C (59°-86°F).*

FDA Label Image

Figure1 (Tramadol Fig1)

A concentration versus time pharmacokinetic curve showing levels of Tramadol and its metabolite M1 after single and multiple doses. The x-axis represents time in hours (up to 48 hours), and the y-axis shows concentration in ng/mL. Different line styles differentiate Tramadol and M1 under single and multiple dosing conditions.*

FDA Label Image

Clinical Studies Section (Tramadol Fig2)

A line graph titled 'Protocol CAPSS-047 Time to Discontinuation Due to Nausea/Vomiting' depicting percent discontinuing on the y-axis and days in double-blind on the x-axis. It compares two dose escalation regimens, 10 days to 200 mg/day (solid line) and 16 days to 200 mg/day (dashed line), showing a higher discontinuation rate for the faster escalation.*

FDA Label Image

Structure (Tramadol Str)

Chemical structure of Tramadol Hydrochloride showing its molecular arrangement including rings, hydroxyl group, methoxy group, and hydrochloride chloride component.*

* 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.