Tramadol Hydrochloride
Product Images NDC 68134-402

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Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Tramadol Hydrochloride (NDC 68134-402). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Palmetto 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.

Product Images & Figures Index

FDA Label Image

Chemical Structure (Figure 01)

Chemical Structure (Figure 01)
FDA Label Image

Figure 1 (Figure 02)

Figure 1 (Figure 02)
FDA Label Image

Figure 2 (Figure 03)

Figure 2 (Figure 03)
The text represents a chart or graph showing the percentage of participants discontinuing a certain protocol (CAPSS-047) due to nausea and vomiting, over a period of 25 days in a double-blind study. The percentage of discontinuing participants ranges from 2% to 50%, and the chart appears to show how often participants discontinued the protocol during specific time frames.*
FDA Label Image

5 mL Unit Dose Cup (Figure 04)

5 mL Unit Dose Cup (Figure 04)
This is a description of a medication labeled with NDC code 68134-402-05 used for institutional purposes only. The medication is an oral solution containing 5mg of Tramadol hydrochloride per 1mL. The net contents of the bottle is 5mL and was manufactured for Palmetto Pharmaceuticals Inc. located in Greenville, SC. The lot number is provided along with an expiration date, but is not visible in the given text.*
FDA Label Image

Case Containing 40 5 mL Unit Dose Cup (Figure 05)

Case Containing 40 5 mL Unit Dose Cup (Figure 05)
This is a description of a Tramadol Hydrochloride oral solution manufactured by Palmetto Pharmaceuticals. The solution contains 5mg/mg and is available in four trays of ten 5mL doses. It should be stored at 20°C to 25°C with excursions permitted to 15°C to 30°C. The product is intended for institutional use only and comes with an NDC number of 68134-402-40. SP-PC-0121.00 and 310114-01 Rev. 03/21 are also mentioned on the label.*

* 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.