Oxycodone And Acetaminophen
Product Images NDC 66336-147

3 FDA label images from Dispensing Solutions, Inc. · 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 And Acetaminophen (NDC 66336-147). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Dispensing Solutions, 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

Ndc 66336-0147-xx (Ndc 66336 0147 Xx Mallinckrodt Inc)

Ndc 66336-0147-xx (Ndc 66336 0147 Xx      Mallinckrodt Inc)
Label for Oxycodone and Acetaminophen 10 mg/325 mg tablets by Dispensing Solutions, Inc. The label includes the NDC 66336-0147 and product number 016-XX. Tablets are white to off-white caplet-shaped, debossed, and supplied in a tight/light-resistant container. The label contains warnings about habit forming use, drowsiness, and advises against alcohol consumption.*
FDA Label Image

Chemical Structure (Oxycodone And Acetaminophen Tablets 01)

Chemical Structure (Oxycodone And Acetaminophen Tablets 01)
Chemical structure of oxycodone hydrochloride, showing the molecular configuration including hydroxyl, methyl, methoxy groups, and hydrochloride salt with molecular formula C18H21NO4·HCl and molecular weight 351.82.*
FDA Label Image

Chemical Structure (Oxycodone And Acetaminophen Tablets 02)

Chemical Structure (Oxycodone And Acetaminophen Tablets 02)
Chemical structure of Oxycodone and Acetaminophen's active ingredient, showing molecular connectivity and functional groups, with molecular formula C8H9NO2 and a molecular weight of 151.16.*

* 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.