Exalgo
Product Images NDC 16590-942

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 Exalgo (NDC 16590-942). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Stat Rx Usa Llc, 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

Label Image 8 mg (Exalgo Er 8mg Label 942)

Label Image 8 mg (Exalgo Er 8mg Label 942)
EXALGO ER C-II 8mg extended-release tablets, 30 count, distributed by STAT Rx USA LLC. The label identifies the product as a generic for Hydromorphone HCL 8mg. The NDC is 16590-942-30. The label also includes dosage information, storage instructions, and regulatory warnings.*
FDA Label Image

Chemical Structure (Exalgo Chem Structure)

Chemical Structure (Exalgo Chem Structure)
Chemical structure of hydromorphone hydrochloride, the active ingredient in EXALGO by STAT Rx USA LLC.*
FDA Label Image

Figure 1 (Exalgo Figure 1)

Figure 1 (Exalgo Figure 1)
A line graph comparing plasma hydromorphone concentrations (ng/mL) over time (hours) for EXALGO 16 mg every 24 hours and HMIR 4 mg every 6 hours. The graph shows fluctuations in drug concentration levels for both dosing regimens between 96 and 120 hours.*
FDA Label Image

Figure 2 (Exalgo Figure 2)

Figure 2 (Exalgo Figure 2)
A line graph comparing the percentage of patients improved over a range of pain reduction percentages from 0 to 100%. Two data series are shown: EXALGO Week 12 represented by black squares, and Placebo Week 12 represented by gray circles. The y-axis indicates patients improved in percentage, and the x-axis shows percent of reduction/improvement in pain.*

* 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.