Oxycodone And Acetaminophen Tablet
Product Images NDC 63187-721

3 FDA label images from Proficient Rx Lp · 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 63187-721). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Proficient Rx Lp, 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

Bf726d0f-figure-01 (Oxycodone And Acetaminophen Tablets Usp 10 mg 325 1)

Bf726d0f-figure-01 (Oxycodone And Acetaminophen Tablets Usp 10 mg 325  1)
Chemical structure of oxycodone hydrochloride showing molecular formula C18H21NO4 with hydrochloride and molecular weight 351.82.*
FDA Label Image

Bf726d0f-figure-02 (Oxycodone And Acetaminophen Tablets Usp 10 mg 325 2)

Bf726d0f-figure-02 (Oxycodone And Acetaminophen Tablets Usp 10 mg 325  2)
Chemical structure diagram showing the molecular structure of Acetaminophen, including functional groups and molecular weight (MW) of 151.17. The image depicts atoms and bonds representing its chemical composition.*
FDA Label Image

63187-721-30 (Oxycodone And Acetaminophen Tablets Usp 10 mg 325 3)

63187-721-30 (Oxycodone And Acetaminophen Tablets Usp 10 mg 325  3)
Label for Oxycodone 10 mg / Acetaminophen (APAP) 325 mg tablets, 60 count, manufactured by Amneal Pharmaceuticals of NY and packaged by Proficient Rx LP. The label includes the NDC 63187-721-60, states "Rx Only" with a C-II controlled substance warning, and describes the tablets as white to off-white, capsule-shaped, biconvex with debossed "IP204" on one side.*

* 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.