Oxycodone And Acetaminophen Tablet
Product Images NDC 72865-116

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Oxycodone And Acetaminophen (NDC 72865-116). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Xlcare Pharmaceuticals, Inc., 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

10 mg 100s

The label for Oxycodone and Acetaminophen Tablets, USP 10 mg/325 mg by XLCare Pharmaceuticals, Inc. It includes dosage details, a note that multiple strengths exist, dispensing instructions, quantity of 100 tablets, and manufacturer information. The label indicates that a DEA order form is required and provides storage conditions.*

FDA Label Image

10 mg 500s

Label for Oxycodone and Acetaminophen Tablets, USP 10 mg*/325 mg by XLCare Pharmaceuticals, Inc. The oral tablet packaging contains 500 tablets. The label states this is a bulk package not child-resistant and includes dosage and storage instructions, manufacturer information, and a note that DEA order form is required. The NDC number is 72865-116-05.*

FDA Label Image

2.5 mg 100s

Label for Oxycodone and Acetaminophen Tablets, USP 2.5 mg/325 mg by XLcare Pharmaceuticals Inc. The bottle contains 100 tablets with an oral tablet dosage form. The label includes dosage details, storage instructions, and manufacturing information. It states the product is Rx only and indicates multiple strengths are available but specifies this label is for the 2.5 mg/325 mg strength.*

FDA Label Image

2.5 mg 500s

Oxycodone and Acetaminophen Tablets USP label from XL Care Pharmaceuticals Inc., showing a strength of 2.5 mg oxycodone and 325 mg acetaminophen per tablet. The label indicates a package of 500 oral tablets, marked as not child-resistant. Additional text includes dosing caution, storage conditions, manufacturer details, and a DEA order form requirement.*

FDA Label Image

5 mg 100s

Label for Oxycodone and Acetaminophen Tablets, USP, 5 mg/325 mg, oral tablets. The label indicates 100 tablets per container manufactured by XLCare Pharmaceuticals, Inc. It includes dosage information, storage instructions, DEA order requirement, and manufacturing details for XLCare Pharmaceuticals and Ascent Pharmaceuticals.*

FDA Label Image

5 mg 500s

Label for Oxycodone and Acetaminophen Tablets, USP 5 mg/325 mg by XLCare Pharmaceuticals, Inc. The label indicates the package contains 500 tablets and is not child-resistant. It includes dosage strength details, storage instructions, and manufacturer information, with a note about multiple strengths and dispensing instructions.*

FDA Label Image

7.5 mg 100s

Oxycodone and Acetaminophen Tablets USP 7.5 mg / 325 mg oral tablets label from XLCare Pharmaceuticals, Inc. The package contains 100 tablets. Label highlights strength and includes NDC 72865-115-01, dosage information, storage instructions, and manufacturer details for XLCare Pharmaceuticals and Ascent Pharmaceuticals.*

FDA Label Image

7.5 mg 500s

Packaging label for Oxycodone and Acetaminophen Tablets, USP 7.5 mg/325 mg, oral tablet by XLCare Pharmaceuticals, Inc. The label indicates 500 tablets in a bulk package that is not child-resistant. It includes dosage strength, DEA order form requirement, storage instructions, and manufacturer information.*

FDA Label Image

Struct1

Chemical structure of oxycodone hydrochloride, showing its molecular formula C18H21NO4·HCl and molecular weight 351.82.*

FDA Label Image

Struct2

Chemical structure of acetaminophen, showing its molecular formula C8H9NO2 and molecular weight 151.17, with labeled functional groups including an amide, hydroxyl, and benzene ring.*

* 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.