Oxycodone Hydrochloride Tablet
Product Images NDC 71335-2126

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Oxycodone Hydrochloride (NDC 71335-2126). 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

Fig 1 (Fig1)

A line graph titled Oxycodone Dose-Proportionality Study showing concentration (ng/mL) over time (hours) for single doses of oxycodone hydrochloride at 5 mg, 15 mg, and 30 mg (6 tablets). The graph displays concentration decreasing over approximately 25 hours, with higher doses corresponding to higher initial concentrations and longer duration.*

FDA Label Image

Structure (Struct)

Chemical structure of Oxycodone Hydrochloride showing its molecular formula C18H21NO4·HCl and molecular weight of 351.82.*

FDA Label Image

Tab 2 (Tab2)

A pharmacokinetic parameters table showing mean and standard deviation values for oxycodone hydrochloride in various dosage forms and doses, including 5 mg and 15 mg tablets, 15 mg oral solution, and 30 mg tablets. It includes parameters such as AUC, Cmax, Tmax, and half-life, and covers single dose, food-effect single dose, and multiple-dose studies.*

FDA Label Image

Label (Lbl713352126)

Label for Oxycodone Hydrochloride 30 mg (CII) tablet, an oral prescription drug packaged by Bryant Ranch Prepack in Burbank, CA. The label includes warnings about overdose and addiction, storage instructions at 20°-25°C (68°-77°F), and urges keeping drugs out of children's reach. The package contains 60 tablets and displays the NDC 71335-2126.*

* 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.