Percocet Tablet
Product Images NDC 72189-397

3 FDA label images from Direct_rx · 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 Percocet (NDC 72189-397). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Direct_rx, 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

72189-397-30 (72189 397 30)

72189-397-30 (72189 397 30)
Packaging label for Percocet Oxycodone/APAP 10 mg/325 mg oral tablets. The label indicates a package containing 30 tablets and states the active ingredients as oxycodone hydrochloride USP and acetaminophen USP, both 325 mg. The labeler is Direct_Rx, and the product NDC is 72189-397. Additional label text includes handling instructions, lot and sample information, and regulatory disclaimers.*
FDA Label Image

72189-397-60 (72189 397 60)

72189-397-60 (72189 397 60)
Percocet Oxycodone/APAP C-II 10/325 mg oral tablets, 60 count bottle labeled as a generic for Percocet. The label states each tablet contains 10 mg Oxycodone Hydrochloride and 325 mg Acetaminophen. Packaged and distributed by Direct Rx in Dawsonville, GA.*
FDA Label Image

72189-397-72 (72189 397 72)

72189-397-72 (72189 397 72)
Label for Oxycodone/APAP C-II 10 mg/325 mg tablets, packaged with 120 tablets. The label indicates the product is a generic for Percocet, with each tablet containing 10 mg of oxycodone hydrochloride and 325 mg of acetaminophen. The label also includes warnings about the risk of addiction and abuse and instructions to keep out of reach of children. The product is distributed by DirectRx.*

* 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.