Oxycodone And Acetaminophen
Product Images NDC 50436-3913

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Oxycodone And Acetaminophen (NDC 50436-3913). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Unit Dose Services, 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

1 (Image 1)

HCl stands for Hydrochloric Acid, which is a strong, highly corrosive acid commonly used in industrial processes such as metal cleaning, refining ore, and neutralizing alkaline materials. It is also found in the human digestive system as a gastric acid that aids in digestion. HCl can be dangerous if not handled properly and can cause burns and respiratory issues if inhaled.*

FDA Label Image

1 (Image 2)

FDA Label Image

Label Image (Lbl504362982)

This text appears to be a product label for a medication called OXYCODONE AND ACETAMINOPHEN G. It contains information about the manufacturer, dosage, and lot numbers. Specific information includes the size of the tablet (75MG/325MG) and the number of tablets in the bottle (30). There are also mentions of manufacturing information such as the batch numbers and the expiration date.*

FDA Label Image

Label Image (Lbl504362983)

FDA Label Image

Label Image (Lbl504363913)

This is a description of a medication with the NDC code 50436-3913-5. It is a combination of Oxycodone and Acetaminophen in a concentration of 5 mg/325 mg. The medication comes in a container with 24 tablets, manufactured by Warner Chilcott Company and packaged by Unit Dose Services, LLC. The medication is for prescription-only and may be used for pain relief. The text also includes various codes related to the medication.*

* 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.