Oxybutynin Chloride Tablet
Product Images NDC 72789-417

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 Oxybutynin Chloride (NDC 72789-417). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pd-rx 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

72789417 Label (72789417)

72789417 Label (72789417)
Label for Oxybutynin Chloride USP 5 mg oral tablets, containing 90 tablets per package. The label shows the NDC 72789-417-90 and is distributed by PD-Rx Pharmaceuticals, Inc., Oklahoma City, OK. It includes dosage strength, quantity, lot number F24D59, expiration date 01/2026, and a warning to keep out of reach of children.*
FDA Label Image

Figure 1 (Oxybutynin Figure1)

Figure 1 (Oxybutynin Figure1)
A line graph depicting the mean plasma concentration of R-Oxybutynin (ng/mL) over a 24-hour period following administration of Oxybutynin 5 mg TID. The X-axis represents time in hours, while the Y-axis represents drug concentration. Concentration peaks appear approximately every 8 hours, reflecting thrice-daily dosing.*
FDA Label Image

Figure 2 (Oxybutynin Figure2)

Figure 2 (Oxybutynin Figure2)
A line graph showing mean R-Oxybutynin plasma concentration (ng/mL) over time (hours). The graph depicts plasma concentration peaking early within 2 hours after administration and then gradually decreasing to near baseline by 12 hours, with error bars indicating variability at each time point.*
FDA Label Image

Structure (Oxybutynin Structure)

Structure (Oxybutynin Structure)
Chemical structure of Oxybutynin Chloride showing the molecular arrangement of its atoms and bonds, including aromatic rings and functional groups as part of its formula.*

* 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.