Oxybutynin Chloride Tablet
Product Images NDC 71335-1014

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Oxybutynin Chloride (NDC 71335-1014). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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 (Lbl713351014)

Label Image (Lbl713351014)
Label of Oxybutynin Chloride 5 mg oral tablets by Bryant Ranch Prepack. The white label includes the product name, strength, dosage form, comparison to Ditropan 5 mg tablets, and storage instructions to keep in a light-resistant container at room temperature. The package contains 30 tablets and displays an NDC barcode and code 71335-1014.*
FDA Label Image

Figure 1 (Oxybutynin Figure1)

Figure 1 (Oxybutynin Figure1)
A line graph displaying the mean plasma concentration of R-Oxybutynin (ng/mL) over a 24-hour period after administering Oxybutynin 5 mg three times daily (TID). The x-axis represents time in hours from 0 to 24, and the y-axis shows mean plasma concentration ranging from 0 to 5 ng/mL, with three distinct peaks corresponding to dosing times.*
FDA Label Image

Figure 2 (Oxybutynin Figure2)

Figure 2 (Oxybutynin Figure2)
A line graph depicting mean R-Oxybutynin plasma concentration (ng/mL) on the y-axis versus time (hours) on the x-axis. The graph shows a peak concentration occurring between 1 and 2 hours, followed by a gradual decline to near baseline levels by 12 hours. Data points include error bars representing variability.*
FDA Label Image

Structure (Oxybutynin Structure)

* 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.