Oxycodone Hydrochloride Tablet
Product Images NDC 71335-2816

View Photos of 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 71335-2816). 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

Structure (740af3a1 1e85 4f74 80d9 13f2f01c878f 01)

Structure (740af3a1 1e85 4f74 80d9 13f2f01c878f 01)
Chemical structure diagram of oxycodone hydrochloride showing the molecular framework with atoms and bonds, including the hydrochloride component. The molecular formula C18H21NO4·HCl and molecular weight 351.82 are also displayed.*
FDA Label Image

Graph (740af3a1 1e85 4f74 80d9 13f2f01c878f 02)

Graph (740af3a1 1e85 4f74 80d9 13f2f01c878f 02)
A line graph titled 'Oxycodone Hydrochloride Tablets Dose-Proportionality Study 5 mg, 15 mg and 30 mg (single-dose)'. It depicts plasma concentration (ng/mL) over time (hours) for different doses of oxycodone: 5 mg x 1, 5 mg x 3, and 5 mg x 6. Concentration peaks early and declines over 24 hours, with higher doses showing higher peaks.*
FDA Label Image

Label (Lbl713352816)

Label (Lbl713352816)
Label for Oxycodone Hydrochloride Tablets USP 30 mg, oral tablets, NDC 71335-2816-1. Contains 60 tablets. Labeler is Bryant Ranch Prepack, repackaged by Bryant Ranch Prepack Inc., Burbank, CA, and manufactured by Strides Pharma Global Pte Ltd. Includes storage instructions, a barcode, and a QR code for package insert.*

* 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.