Oxybutynin Chloride
Product Images NDC 42291-914

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Oxybutynin Chloride (NDC 42291-914). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Avkare, 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

500 (914 50)

Oxybutynin Chloride Tablets USP 5 mg by AvKARE, showing a label for a bottle containing 500 tablets. The label includes the product name, strength, quantity, Rx only designation, NDC 42291-914-50, and storage instructions. A QR code and barcode are also visible on the label.*

FDA Label Image

Structural Formula (A8b5b863 6c18 4dcc 92e0 C1fa99cff42b 01)

Chemical structure of oxybutynin chloride is shown, illustrating its molecular framework including a benzene ring, alkyne group, ester linker, and the diethylamino functional group bound to chloride.*

FDA Label Image

Graph 1 (A8b5b863 6c18 4dcc 92e0 C1fa99cff42b 02)

A line graph depicting the mean R-Oxybutynin plasma concentration over time in hours. The y-axis shows concentration in ng/mL ranging from 0 to 10, and the x-axis shows time points from 0 to 12 hours. Data points show a decreasing trend in concentration over time with error bars indicating variability.*

FDA Label Image

Graph 2 (A8b5b863 6c18 4dcc 92e0 C1fa99cff42b 03)

A line graph depicting mean R-Oxybutynin plasma concentration (ng/mL) over time (hours). The graph shows a decline in concentration from approximately 6 ng/mL at 0 hours down to about 1 ng/mL at 8 hours, with an additional data point at 12 hours. Error bars indicate variability at each time point.*

* 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.