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)

This is a label of a bottle of Tramadol Hydrochloride Tablets, USP. The tablets are 50 MG each and the bottle contains 9 tablets. It was manufactured by Rising Pharma Holdings in India and packaged in Oro Valley, Arizona, USA. It has an NDC number of 60760-772-09 and the lot number is 777227. The expiry date is 22-77 and it should be stored at controlled room temperature between 15°C to 30°C (59°F to 86°F). It also provides information on how to use it and a contact number.*

FDA Label Image

Figure1 (Tramadol Fig1)

FDA Label Image

Clinical Studies Section (Tramadol Fig2)

This is a graph displaying the percentage of participants discontinuing Protocol CAPSS-047 due to nausea and vomiting over 10 days and the time to discontinuation. The x-axis represents the number of days in the double-blind period, and the y-axis represents the percentage of participants discontinuing. The graph shows that within the first 10 days of the protocol, over 50% of participants discontinued due to nausea and vomiting at a dosage of 200mg/day.*

FDA Label Image

Structure (Tramadol Str)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.