Oxycodone And Acetaminophen
Product Images NDC 52959-119

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 And Acetaminophen (NDC 52959-119). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by H.j. Harkins Company, 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

50d9d2dc-figure-01 (50d9d2dc Figure 01)

FDA Label Image

50d9d2dc-figure-02 (50d9d2dc Figure 02)

FDA Label Image

50d9d2dc-figure-03 (50d9d2dc Figure 03)

50d9d2dc-figure-03 (50d9d2dc Figure 03)
This is a description of a prescription medication with the National Drug Code (NDC) 52959-119-30, which is only available with a prescription (RX Only). The medication is Oxycodone combined with the pain reliever Acetaminophen in a 10/325mg dosage. The tablets are white with the identification code AXKX00OKK. The manufacturer is AmnealPhrm and the lot number is OAT00QY with an expiration date of February 12th. The medication is similar to Percocet, manufactured in Hauppauge, NY, with an NDC of 53746-204-01. There is a caution on the label to only take the medication as directed by a doctor, and to see the enclosed information for dosage information. There are also various lot numbers listed for this medication, ending with 53746-204-01. Overall, this is a description of a prescription pain medication with specific identifying information.*

* 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.