Oxybutynin Chloride Tablet
Product Images NDC 55154-2632

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Oxybutynin Chloride (NDC 55154-2632). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cardinal Health 107, 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

5mg Bag Label (8455b543 81ce 4522 Ae9b 8396f944945c 00)

Oxybutynin Chloride Tablets USP 5 mg label in a unit dose package containing 10 tablets. The label lists dosing, storage instructions, and warnings, specifying it is for prescription use only and not child resistant. Manufactured by Novitium Pharma LLC and distributed by Major Pharmaceuticals and Cardinal Health.*

FDA Label Image

Graph 1 (Oxybutynin Graph1)

A line graph depicting mean plasma R-oxybutynin concentration (ng/mL) over 24 hours following administration of Oxybutynin 5 mg three times daily (TID). The x-axis represents time in hours, while the y-axis shows plasma concentration. Three distinct peaks correspond to dosing times throughout the day, with error bars indicating variability at each point.*

FDA Label Image

Graph 2 (Oxybutynin Graph2)

A line graph showing mean plasma concentration of Oxybutynin in ng/mL over time in hours. The graph depicts concentration rising sharply shortly after zero time, peaking before 2 hours, then gradually decreasing to near baseline by 12 hours, with error bars indicating variability at each time point.*

FDA Label Image

Structure (Oxybutynin Structure)

Chemical structure diagram of Oxybutynin Chloride showing the molecular arrangement including a cyclohexyl group, phenyl group, ester linkage, ethynyl group, and diethylamine hydrochloride moiety.*

* 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.