Oxycodone Hydrochloride Tablet
Product Images NDC 60760-957

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 Oxycodone Hydrochloride (NDC 60760-957). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by St. Mary's Medical Park Pharmacy, 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

957-60 (Oxycodone 60760 957 60)

957-60 (Oxycodone 60760 957 60)
Label for Oxycodone Hydrochloride Tablets, USP 15 mg, with a quantity of 60 tablets. The label indicates the product is manufactured by KVK-Tech, Inc., Newtown, PA, and packaged by St. Mary's Medical Park Pharmacy in Oro Valley, AZ. It includes regulatory identifiers such as NDC 60760-957-60 and controlled substance classification 'CII.' Expiry date, lot number, and prescription number fields are shown as placeholders.*
FDA Label Image

Chemical Structure (Figure 1 Chemical Structure)

Chemical Structure (Figure 1 Chemical Structure)
Chemical structure of oxycodone hydrochloride, showing its molecular formula C18H21NO4·HCl and molecular weight (MW) 351.82.*
FDA Label Image

Figure1 (Figure 2 Fig1 Graph)

Figure1 (Figure 2 Fig1 Graph)
Line graph showing the dose-proportionality study of oxycodone hydrochloride at 5 mg dosage given once, three times, and six times. The y-axis represents oxycodone plasma concentration (ng/mL), and the x-axis shows time in hours up to 25 hours, illustrating increasing concentration peaks with higher dosing.*
FDA Label Image

* 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.