Oxycodone And Acetaminophen
Product Images NDC 67296-1392

3 FDA label images from Redpharm Drug, Inc. · 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 67296-1392). 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.

Product Images & Figures Index

FDA Label Image

67296 1392

67296 1392
Multiple labels for Oxycodone HCL & Acetaminophen 5/325MG tablets in various tablet counts including 4, 6, 10, 15, 20, 30, 40, 50, and 60 tablets. Each label shows Rx only, lot number, expiration date, manufacturer (Aurobindo Pharma USA Inc., Dayton NJ), distributor (Redpharm Drug, Eden Prairie MN), storage instructions, and barcodes.*
FDA Label Image

Oxyapap 67296 1392 9

Oxyapap 67296 1392 9
Label for Oxycodone HCl and Acetaminophen tablets, strength 5/325 mg, containing 4 tablets. The label indicates Rx only, includes lot number 8020A1X1 and expiration date 11/20. Manufactured by Aurobindo Pharma USA Inc, Dayton NJ, and distributed by RedPharm Drug, Eden Prairie MN. The label also shows storage instructions for controlled room temperature (20-25°C).*
FDA Label Image

Oxy/apap 5/325 (Doc20170526144506 001)

Oxy/apap 5/325 (Doc20170526144506 001)
Labels for Oxycodone HCL & Acetaminophen 5/325MG tablets in various tablet counts including 6, 10, 12, 15, 20, 30, 50, and 60 tablets. Each label includes NDC numbers, lot numbers, expiration date 08/18, and storage instructions at 20-25°C (68-77°F). Manufactured by Aurolife Pharma LLC, distributed by RedPharm Drug, Inc., Eden Prairie, MN.*

* 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.