Oxybutynin Chloride Tablet
Product Images NDC 51407-099

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Oxybutynin Chloride (NDC 51407-099). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Golden State Medical Supply, 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.

FDA Label Image

Spl (51407-099-01LB)

Label for Oxybutynin Chloride tablets, USP 5 mg, packaged as 100 tablets. The label includes the NDC 51407-099-01 and indicates the product is prescription only (Rx only). The labeler is Golden State Medical Supply, Inc., with storage instructions at 20 to 25°C. Additional handling and administration warnings are partially visible.*

FDA Label Image

Graph 1 (Oxybutynin Graph1)

A line graph showing mean plasma concentration of oxybutynin (ng/mL) over 24 hours after oral administration of Oxybutynin Chloride 5 mg taken three times daily (TID). The x-axis represents time in hours, and the y-axis represents mean plasma R-oxybutynin concentration, with three distinct peaks corresponding to dosing times.*

FDA Label Image

Graph 2 (Oxybutynin Graph2)

A line graph depicting the mean plasma concentration of Oxybutynin over a 12-hour period. The x-axis represents time in hours, and the y-axis shows mean Oxybutynin plasma concentration in ng/mL. Data points include error bars indicating variability at each time interval, showing a peak around 1-2 hours followed by a decline.*

FDA Label Image

Structure (Oxybutynin Structure)

Chemical structure of oxybutynin chloride, illustrating its molecular framework with associated hydrochloride component as shown in the diagram.*

* 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.