Tramadol Hydrochloride Tablet
Product Images NDC 68071-3644

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 68071-3644). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Nucare 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

Pdp (68071 3644 9)

Pdp (68071 3644 9)
Label for NuCare Pharmaceuticals tramadol hydrochloride 50 mg tablets, oral dosage form. The label indicates a package size of 90 tablets, capsule-shaped white tablets debossed with "ET50". It includes NDC code 68071-3644, manufacturer details, and controlled substance schedule IV marking. Storage instructions and warnings are also shown.*
FDA Label Image

Figure 1 (Tramadol 02)

Figure 1 (Tramadol 02)
A line graph showing the concentration (ng/mL) of tramadol and its M1 metabolite over time (hours). Four curves compare tramadol and M1 levels after multiple dose and single dose administration, illustrating pharmacokinetic profiles up to 48 hours post-dose.*
FDA Label Image

Figure 2 (Tramadol 03)

Figure 2 (Tramadol 03)
A line chart titled 'Protocol CAPSS-047' showing percentage discontinuation over 25 days due to nausea/vomiting in a double-blind study. The chart compares two treatment durations to 200 mg/day: 10 days (red solid line) and 16 days (blue dashed line), with the 10-day group showing higher discontinuation rates over time.*
FDA Label Image

Structure (Tramadol 1)

Structure (Tramadol 1)
Chemical structure of tramadol hydrochloride showing its molecular configuration with functional groups and the hydrochloride 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.