Oxycodone And Acetaminophen Tablet
Product Images NDC 68084-710

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Oxycodone And Acetaminophen (NDC 68084-710). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by American Health Packaging, 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

0269901 0721 Oxycodone Apap 7 5 325mg 10x10 V1 Final Image

Label for Oxycodone and Acetaminophen tablets, USP 7.5 mg/325 mg, containing 100 tablets (10 x 10), indicated for oral use. The label includes NDC 68084-699-01 and states Rx only. It provides pharmacist instructions and dosage details. Distributed by American Health Packaging, Columbus, Ohio.*

FDA Label Image

0271001 0121 Oxycodone Apap 10 325mg 10x10 V2 Final Image

Label for Oxycodone and Acetaminophen Tablets USP, 10 mg/325 mg strength, oral tablets. The label indicates a package size of 100 tablets (10x10) and is marked for prescription use only. It includes the DEA Schedule II symbol and notes the product is distributed by American Health Packaging, Columbus, Ohio.*

FDA Label Image

87.5 mg 10 mg Blister

The image shows multiple medication labels for Oxycodone and Acetaminophen tablets, USP 7.5 mg/325 mg, manufactured by American Health Packaging. Each label includes the product name, strength, dosage form, a barcode, lot number, expiration date field, and labeling information indicating oral route and prescription use.*

FDA Label Image

Ahp69901

Round yellow oral tablet of Oxycodone and Acetaminophen imprinted with "229" on one side and a curved C-shaped logo on the other. Manufactured by American Health Packaging.*

FDA Label Image

Ahp71001

Tablet of Oxycodone and Acetaminophen showing round, yellow tablet with the imprint '230' on one side and a distinctive logo resembling a stylized 'A' on the other side. The product is an oral prescription tablet by American Health Packaging.*

FDA Label Image

Apap Structure

Chemical structure diagram showing a molecule with the formula including CH3CONH, OH attached to a benzene ring, and C8H9NO2, with a molecular weight (MW) of 151.17. This likely represents the active ingredient shown in the product data.*

FDA Label Image

10 mg/325 mg Oxycodone/apap Tablet Blister (Card Print Oxycodone Apap 10mg 325mg)

Label sheet for Oxycodone and Acetaminophen Tablets USP 10 mg/325 mg from American Health Packaging. Each label includes the drug name, dosage strength, NDC barcode, lot number field, expiration date field, and manufacturer information. The labels are arranged in pairs across the sheet for application on individual bottles or containers.*

FDA Label Image

Oxycodone Structure

Chemical structure of Oxycodone hydrochloride, showing molecular formula C18H21NO4 and molecular weight 351.82, including structural bonds, rings, and functional groups typical of the compound.*

FDA Label Image

D77de3aeb01482e6 (C78d66e2 Figure 03)

Oxycodone and Acetaminophen oral tablets packaging label showing two dosage strengths: 10 mg oxycodone with 325 mg acetaminophen, and 7.5 mg oxycodone with 325 mg acetaminophen. The label indicates American Health Packaging as the labeler and displays the tablets in a blister pack format with each dose clearly marked.*

FDA Label Image

D77de3aeb01482e6 (C78d66e2 Figure 04)

Oxycodone and Acetaminophen 7.5 mg / 325 mg oral tablets carton by American Health Packaging. The label displays the product name prominently with active ingredient strengths, dosage form as tablets, and includes standard regulatory and manufacturer information on a white and light teal background.*

* 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.