Oxybutynin Chloride
Product Images NDC 53808-0873

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Oxybutynin Chloride (NDC 53808-0873). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by State Of Florida Doh Central Pharmacy, 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

Label Image For 5mg (Oxybutynin 5mg)

Label for Oxybutynin Chloride 5 mg tablets, quantity 60, prescription only. Packaged by DOH Central Pharmacy, Tallahassee, FL 32304, with an expiration date of January 31, 2013. The label includes a barcode and lists Upsher-Smith as the manufacturer.*

FDA Label Image

Chemical Structure (Oxybutynin 01)

Chemical structure of oxybutynin chloride, showing its molecular composition including a cyclohexanone ring and an ethylamine group with hydrochloride.*

FDA Label Image

Figure (Oxybutynin 02)

A line graph showing mean plasma concentration of Oxybutynin over a 24-hour period after oral dosing at 5 mg three times daily (TID). The x-axis represents time in hours, and the y-axis indicates mean plasma oxybutynin concentration with error bars illustrating variability at each time point.*

FDA Label Image

Figure (Oxybutynin 03)

A line graph depicting the mean R-Oxybutynin plasma concentration (ng/mL) over time (hours). The graph shows data points with error bars ranging from 0 to 12 hours on the x-axis and plasma concentration values from 0 to 10 ng/mL on the y-axis, illustrating a peak concentration shortly after 1 hour and a gradual decline thereafter.*

* 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.