Oxycodone Hcl Tablet
Product Images NDC 72189-632

View Photos of 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 Hcl (NDC 72189-632). 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

72189-632-30 (72189 632 30)

72189-632-30 (72189 632 30)
Label for Oxycodone HCL C-II 10 mg oral tablets, containing 30 tablets. The label states it is generic for Roxicodone and each tablet contains 10 mg of oxycodone hydrochloride. The label includes directions for storage, caution about prescription transfer, and indicates that refills are not permitted without a physician's authorization. Distributed by Direct Rx, with packaging details and lot/sample information also visible.*
FDA Label Image

72189-632-60 (72189 632 60)

72189-632-60 (72189 632 60)
Label for Oxycodone HCL C-II 10 mg oral tablets, containing 60 tablets per bottle. The label identifies the product as a generic for Roxicodone with each tablet containing 10 mg of Oxycodone Hydrochloride. It is packaged and distributed by Direct Rx. The label includes dispensing and storage information, federal caution, refill restrictions, and the NDC 72189-632-60.*
FDA Label Image

72189-632-90 (72189 632 90)

72189-632-90 (72189 632 90)
Label for Oxycodone HCL C-II 10 mg oral tablets, containing 90 tablets per bottle. The label states it is generic for Roxicodone and includes lot number, expiration date, and manufacturer details. Distributed by Direct_Rx, the label also carries caution statements about federal transfer restrictions and prescription use only.*

* 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.