Oxybutynin Chloride Tablet
Product Images NDC 51655-665

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Oxybutynin Chloride (NDC 51655-665). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northwind Health Company, 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.

FDA Label Image

Label (51655 665 25)

Label for Oxybutynin Chloride Tablets, USP 5 mg, containing 60 tablets. The label indicates prescription-only status and storage instructions at controlled room temperature. It is labeled by Northwind Health Company, LLC, and includes dosage form, strength, package count, and handling information.*

FDA Label Image

Graph 1 (Oxybutynin Graph1)

A line graph showing mean plasma oxybutynin concentration (ng/mL) over 24 hours after dosing with 5 mg oxybutynin three times daily (TID). Concentration peaks occur around 1, 8, and 16 hours, with decline phases following each peak. Error bars indicate variability at each time point.*

FDA Label Image

Graph 2 (Oxybutynin Graph2)

A line graph depicting mean oxybutynin plasma concentration (ng/mL) over 12 hours. The x-axis represents time (hours) from 0 to 12, while the y-axis shows plasma concentration from 0 to 10 ng/mL. Data points with error bars indicate plasma concentration peaks around 2 hours, followed by a decline to near baseline by 12 hours.*

FDA Label Image

Structure (Oxybutynin Structure)

Chemical structure of Oxybutynin Chloride, showing the molecular arrangement of atoms including aromatic rings, ester and amide linkages, an alkyne group, and the hydrochloride salt form indicated by HCl.*

* 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.