Oxycodone And Acetaminophen Tablet
Product Images NDC 60760-899

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Oxycodone And Acetaminophen (NDC 60760-899). 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

60760-899 (Oxycodone 60760 899 90)

Label for Oxycodone and Acetaminophen Tablets, USP, 10 mg/325 mg, oral tablet form. The label indicates a quantity of 90 tablets, with a National Drug Code (NDC) of 60760-899-90, manufactured by Alvogen, Inc., and packaged by St. Mary's Medical Park Pharmacy. It includes storage instructions to keep at controlled room temperature 15°-30°C (59°-86°F) and a cautionary note to use as directed and Rx only.*

FDA Label Image

Alvogen-logo-2 (Alvogen Logo 2)

Packaging label for Oxycodone and Acetaminophen tablets, oral route, showing dosage strengths of 325 mg and 10 mg. The label includes the name of the labeler, St. Mary's Medical Park Pharmacy, and features barcodes and standard drug packaging information on a white background.*

FDA Label Image

Apap-structure (Apap Structure)

Chemical structure diagram showing a molecule with a benzene ring substituted with an acetamide group (CH3CONH) and a hydroxyl group (OH). The molecular formula is C8H9NO2 with a molecular weight of 151.17.*

FDA Label Image

Oxy-hcl-structure (Oxy HCl Structure)

Chemical structure of oxycodone hydrochloride, showing the molecular formula C18H21NO4·HCl and molecular weight 351.82, with the characteristic fused ring system and functional groups.*

* 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.