Oxycodone Hydrochloride Tablet
Product Images NDC 60760-955

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 60760-955). 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

60760-955 (Oxycodone 60760 955 60)

60760-955 (Oxycodone 60760 955 60)
Oxycodone Hydrochloride 10 mg tablets packaging label from St. Mary's Medical Park Pharmacy. The label displays the drug name, strength, dosage form (tablet), quantity of 60 tablets, and includes various lot, expiration, and NDC information with placeholders. It also includes storage instructions to keep at controlled room temperature, a barcode, and the manufacturer's details.*
FDA Label Image

Chemical Structure (Figure 1 Chemical Structure)

Chemical Structure (Figure 1 Chemical Structure)
Chemical structure of oxycodone hydrochloride. The diagram displays the molecular structure with labeled chemical groups and includes the molecular weight (MW 351.82) and molecular formula (C18H21NO4·HCl).*
FDA Label Image

Figure1 (Figure 2 Fig1 Graph)

Figure1 (Figure 2 Fig1 Graph)
A line graph titled 'Oxycodone Hydrochloride Dose-Proportionality Study' showing concentration (ng/mL) over time (hours) for single doses of 5 mg, 15 mg, and 30 mg oxycodone. The graph compares three curves representing 5 mg x 1, 5 mg x 3, and 5 mg x 6 doses, illustrating drug concentration decline over approximately 25 hours.*
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.