Oxycodone Hydrochloride Tablet
Product Images NDC 60760-954

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 60760-954). 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

60760-954 (Oxycodone 60760 954 30)

60760-954 (Oxycodone 60760 954 30)
Label for Oxycodone Hydrochloride Tablets USP 5mg, oral tablets, with NDC 60760-954-30. The label shows a quantity of 30 tablets and includes placeholder text for lot number and expiration date. It indicates the product is manufactured by KVK-Tech, Inc. in Newtown, PA, and packaged by St. Mary's Medical Park Pharmacy in Oro Valley, AZ. The label contains storage instructions to store at controlled room temperature (15°-30°C).*
FDA Label Image

Chemical Structure (Figure 1 Chemical Structure)

Chemical Structure (Figure 1 Chemical Structure)
Chemical structure of oxycodone hydrochloride showing the molecular arrangement with its chemical formula C18H21NO4.HCl and molecular weight 351.82.*
FDA Label Image

Figure1 (Figure 2 Fig1 Graph)

Figure1 (Figure 2 Fig1 Graph)
A line graph titled 'Oxycodone Hydrochloride Dose-Proportionality Study 5 mg, 15 mg and 30 mg (single-dose)' showing concentration of oxycodone (ng/mL) on the y-axis versus time (hours) on the x-axis. Three lines represent different dose equivalents: 5 mg x 1, 5 mg x 3, and 5 mg x 6, depicting the concentration over a 25-hour period.*
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.