Ibuprofen Tablet
Product Images NDC 53746-465

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Ibuprofen (NDC 53746-465). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal Pharmaceuticals Of New York Llc, 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

56fb8872-figure-01 (Ibuprofen Tablets Usp 1)

Chemical structure diagram of ibuprofen, showing the benzene ring and side chains typical of the ibuprofen molecule.*

FDA Label Image

100 Ct. (Ibuprofen Tablets Usp 2)

Label for Ibuprofen Tablets USP 400 mg oral tablets by Amneal Pharmaceuticals of New York LLC. The package contains 100 film-coated tablets. The label includes storage instructions, pharmacist dispensing guidance, and a QR code for the medication guide. The product is prescription-only.*

FDA Label Image

100 Ct. (Ibuprofen Tablets Usp 3)

Label for Ibuprofen Tablets USP 600 mg by Amneal Pharmaceuticals of New York LLC. The label states 'Rx only' and indicates a package size of 100 tablets. It includes instructions for pharmacists to dispense the medication guide to patients, storage conditions, and a barcode. The label also provides a QR code linking to the medication guide.*

FDA Label Image

100 Ct. (Ibuprofen Tablets Usp 4)

Label for Ibuprofen Tablets, USP 800 mg by Amneal Pharmaceuticals of New York LLC. The label shows the strength as 800 mg, the form as tablets, and indicates it is Rx only. It includes instructions for the pharmacist to dispense the medication guide to each patient and storage information, along with a QR code and barcode.*

* 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.