Oxybutynin Chloride Tablet
Product Images NDC 0832-0038

4 FDA label images from Upsher-smith Laboratories, Llc · 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 Oxybutynin Chloride (NDC 0832-0038). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Upsher-smith Laboratories, 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

Chemical Structure (Oxybutynin 01)

Chemical Structure (Oxybutynin 01)
Chemical structure of Oxybutynin Chloride showing its molecular arrangement with benzene ring, cyclohexyl group, ester linkage, ethynyl group, diethylamino moiety, and hydrochloride salt.*
FDA Label Image

Figure 1 (Oxybutynin 02)

Figure 1 (Oxybutynin 02)
A line graph depicting the mean plasma R-Oxybutynin concentration (ng/mL) over 24 hours after administration of Oxybutynin 5 mg three times daily (TID). The x-axis shows time in hours (0 to 24), and the y-axis shows the concentration levels, with data points connected by a line and error bars indicating variability at each time point.*
FDA Label Image

Figure 2 (Oxybutynin 03)

Figure 2 (Oxybutynin 03)
A line graph depicting the mean R-Oxybutynin plasma concentration (ng/mL) over time (hours). The y-axis shows plasma concentration ranging from 0 to 10 ng/mL, while the x-axis shows time points from 0 to 12 hours. The graph includes error bars at each data point, indicating variability in the measurements.*
FDA Label Image

Principal Display Panel (5 mg Tablet Blister Pack Carton)

Principal Display Panel (5 mg Tablet Blister Pack Carton)
The packaging label for Oxybutynin Chloride Tablets, USP 5 mg by Upsher-Smith Laboratories, LLC shows a carton for 100 unit-dose tablets (10 x 10). The label includes the product name, strength, NDC 0832-0038-01, manufacturer information, a barcode, and storage instructions. It notes the unit-dose package is not child-resistant and intended for institutional use only.*

* 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.