Oxycodone Hydrochloride Tablet
Product Images NDC 71335-0677

3 FDA label images from Bryant Ranch Prepack · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Oxycodone Hydrochloride (NDC 71335-0677). 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.

Product Images & Figures Index

FDA Label Image

Lbl7133506772

Lbl7133506772
Oxycodone Hydrochloride 30 mg tablet label from Bryant Ranch Prepack. The label identifies the product as a Schedule II controlled tablet comparable to Roxicodone 30 mg by Amneal Pharmaceuticals LLC. It includes storage instructions, a caution about overdose risk, and states the quantity as 60 tablets with NDC 71335-0677. The label features a barcode and a lot number.*
FDA Label Image

Formula (Oxycodone Hydrochloride Tablets Usp 1)

Formula (Oxycodone Hydrochloride Tablets Usp 1)
Chemical structure of Oxycodone Hydrochloride showing its molecular formula C18H21NO4 and molecular weight 351.82. The diagram includes atom groups and bonds typical for the oxycodone molecule with an HCl component.*
FDA Label Image

Figure 1 (Oxycodone Hydrochloride Tablets Usp 2)

Figure 1 (Oxycodone Hydrochloride Tablets Usp 2)
A line graph depicting concentration of Oxycodone (5 mg) in the body over time (hours) for three dosing regimens: a single dose, three doses, and six doses. The graph shows concentration decreasing gradually over a 24-hour period, with higher peaks and longer duration for multiple dosing.*

* 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.