Oxycodone Hydrochloride Tablet
Product Images NDC 42858-001

7 FDA label images from Rhodes Pharmaceuticals Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Oxycodone Hydrochloride (NDC 42858-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rhodes Pharmaceuticals 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

Chemical Structure (Oxy 01)

Chemical Structure (Oxy 01)
Chemical structure of Oxycodone Hydrochloride showing its molecular bonds and functional groups, including aromatic rings, hydroxyl (OH), methoxy (CH3O), and other substituents along with the hydrochloride (HCl) moiety.*
FDA Label Image

Figure 1 (Oxy 02)

Figure 1 (Oxy 02)
A pharmacokinetic concentration-time graph showing oxycodone levels in ng/mL over 25 hours after oral administration. The chart compares three dosages of 5 mg oxycodone tablets: single dose, three doses, and six doses, illustrating concentration changes over time.*
FDA Label Image

Principal Display Panel (5 mg Tablet Bottle Label)

Principal Display Panel (5 mg Tablet Bottle Label)
Oxycodone Hydrochloride Tablets USP 5 mg, oral tablets, packaged in a 100-tablet bottle. Label states 'Rx Only' and includes dispensing instructions to provide the accompanying Medication Guide to each patient. Marketed by Rhodes Pharmaceuticals L.P., Coventry, RI, and manufactured by Purdue Pharma L.P., Stamford, CT. The label also includes storage conditions and a barcode with NDC 42858-001-01.*
FDA Label Image

Principal Display Panel (10 mg Tablet Bottle Label)

Principal Display Panel (10 mg Tablet Bottle Label)
Oxycodone Hydrochloride Tablets USP 10 mg label from Rhodes Pharmaceuticals LLC. The label indicates the product contains 100 tablets, intended for oral use, and is Rx only. It features dosage instructions, storage conditions, and a barcode, along with manufacturer and marketer information.*
FDA Label Image

Principal Display Panel (15 mg Tablet Bottle Label)

Principal Display Panel (15 mg Tablet Bottle Label)
Oxycodone Hydrochloride Tablets USP 15 mg oral tablets label from Rhodes Pharmaceuticals LLC. The label indicates a package of 100 tablets. It includes instructions to dispense an accompanying Medication Guide, storage information, and warnings about moisture protection and unopened tablet identification. NDC 42858-003-01 is visible along with manufacturer details for Purdue Pharma L.P.*
FDA Label Image

Principal Display Panel (20 mg Tablet Bottle Label)

Principal Display Panel (20 mg Tablet Bottle Label)
Label for Oxycodone Hydrochloride Tablets USP 20 mg by Rhodes Pharmaceuticals LLC. The label indicates Rx only status with a package quantity of 100 tablets. Instructions include dispensing the accompanying Medication Guide, storage conditions, and moisture protection directions. The label also shows the National Drug Code (NDC) 42858-004-01 and manufacturer information.*
FDA Label Image

Principal Display Panel (30 mg Tablet Bottle Label)

Principal Display Panel (30 mg Tablet Bottle Label)
Oxycodone Hydrochloride Tablets USP 30 mg oral tablets label from Rhodes Pharmaceuticals LLC. The label states 'Rx Only' and contains 100 tablets. It includes dispensing instructions, storage conditions, a barcode, and manufacturer details (Purdue Pharma L.P., Stamford, CT). The label emphasizes protecting from moisture and carrying proper identification when using the tablets.*

* 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.