Oxycodone Hydrochloride
Product Images NDC 67296-0832

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Oxycodone Hydrochloride (NDC 67296-0832). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Redpharm Drug, 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

Oxy 67296 0832

Two separate labels for Oxycodone Hydrochloride tablets from RedPharm Drug, Inc. One label indicates a 5 mg strength with 4 tablets, the other a 5 mg strength with 6 tablets. Both include lot numbers, expiration date 04/23, storage instructions at 20-25°C, manufacturer KVK-Tech Inc. in Newtown, PA, and distributor RedPharm Drug in Eden Prairie, MN. Each label has barcodes and Rx Only designation.*

FDA Label Image

67296-0832 (Doc20161130153610 001)

Packaging labels for Oxycodone Hydrochloride tablets, USP, 5 mg. The image shows multiple label versions for 10, 20, and 40 tablet counts. The labels include prescription-only designation, lot numbers, expiration dates, and storage instructions. Manufacturer is KVK-Tech Inc., Newtown, PA, distributed by RedPharm Drug, Inc., Eden Prairie, MN. Barcodes and NDC numbers are also visible.*

FDA Label Image

Oxy (Doc20170810133349 001)

Two labels of OXYCODONE HCL 5MG tablets from RedPharm Drug, Inc. Each label shows prescription status (Rx Only), batch lot numbers, expiration date 05/21, and tablet counts of 60 and 80 respectively. Manufacturer is KVK-TECH, INC., Newtown, PA, with distributor address in Eden Prairie, MN. Each label includes a barcode and storage instructions (20-25°C).*

* 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.