Oxycodone Hydrochloride And Acetaminophen Tablet
Product Images NDC 60760-964

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 And Acetaminophen (NDC 60760-964). 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

964-30 (Oxycodone 60760 964 30)

964-30 (Oxycodone 60760 964 30)
Label for Oxycodone Hydrochloride and Acetaminophen Tablets USP 7.5 mg / 325 mg, oral tablets, quantity 30. The label shows multiple small repeating panels with the product name, strength, and quantity, along with placeholder lot and expiration dates. It is packaged by St. Mary's Medical Park Pharmacy in Oro Valley, AZ, and manufactured by Elite Laboratories, Inc., Northvale, NJ. The label includes a barcode, storage instructions for controlled room temperature (15°-30°C), and an Rx only statement.*
FDA Label Image

Acetaminophen Chemical Structure (Acetaminophen Structure)

Acetaminophen Chemical Structure (Acetaminophen Structure)
Chemical structure of Oxycodone Hydrochloride and Acetaminophen showing molecular connections and functional groups relevant to its dual active ingredients.*
FDA Label Image

Opium Alkaloid- Thebaine Structure (Opium Alkaloid Thebaine Structure)

Opium Alkaloid- Thebaine Structure (Opium Alkaloid Thebaine Structure)
Chemical structure diagram of Oxycodone Hydrochloride, showing its molecular framework annotated with hydrogen, oxygen, carbon atoms and the hydrochloride component.*

* 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.