Tramadol Hydrochloride
Product Images NDC 63874-532

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Tramadol Hydrochloride (NDC 63874-532). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Altura Pharmaceuticals, 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.

FDA Label Image

2fd4ba08-figure-01 (2fd4ba08 Figure 01)

Chemical structure of Tramadol Hydrochloride showing its molecular components including a methoxyphenyl group, cyclohexanol ring, and dimethylamino methyl side chain with a hydrochloride moiety.*

FDA Label Image

2fd4ba08-figure-02 (2fd4ba08 Figure 02)

A line graph depicting the concentrations (ng/mL) of Tramadol and its metabolite M1 over time (hours). It compares multiple and single doses of Tramadol and M1, illustrating concentration decreases over a 48-hour period.*

FDA Label Image

2fd4ba08-figure-03 (2fd4ba08 Figure 03)

A stepped line graph showing the percent of patients discontinuing treatment due to nausea or vomiting over 25 days in a double-blind protocol (CAPSS-047). The y-axis represents percent discontinuing, increasing from 0 to 50%, while the x-axis shows days up to 25. The graph is labeled for 10 days to 200 mg/day.*

FDA Label Image

Label Image 50 mg Tablets (63874 0532 33 1)

Tramadol Hydrochloride 50 mg tablets label from Altura Pharmaceuticals, Inc. The label identifies the product as a generic for Ultram with 30 tablets per package. It includes storage information, lot and expiration date placeholders, and a warning to keep out of children's reach. The NDC number 63874-532-33 is shown along with a barcode.*

* 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.