Oxycodone Hcl Tablet
Product Images NDC 72189-614

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 72189-614). 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

72189-614-30 (72189 614 30)

72189-614-30 (72189 614 30)
Oxycodone HCL C-II 15 mg tablet blister pack containing 30 tablets. The label states it is a generic for Roxicodone and each tablet contains 15 mg of oxycodone hydrochloride. The package is distributed by Direct Rx and includes cautions about federal transfer and instructions to keep out of reach of children.*
FDA Label Image

72189-614-60 (72189 614 60)

72189-614-60 (72189 614 60)
Oxycodone HCL C-II 15 mg oral tablets, 60 count. The label indicates this product is generic for Roxicodone and each tablet contains 15 mg of Oxycodone Hydrochloride, USP. It is manufactured or distributed by Direct Rx, packaged in Dawsonville, GA. The label includes regulatory warnings about RX-only status, storage instructions, and a lot number with expiration date.*
FDA Label Image

72189-614-90 (72189 614 90)

72189-614-90 (72189 614 90)
Oxycodone HCL C-II 15 mg oral tablets, 90 count, packaged and distributed by Direct Rx in Dawsonville, GA. The label indicates the product is generic for Roxicodone and each tablet contains 15 mg of oxycodone hydrochloride. The package includes lot number, expiration date of 07/31/26, and cautionary information regarding prescription and child safety.*

* 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.