Rufinamide Tablet, Film Coated
Product Images NDC 59651-616

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 Rufinamide (NDC 59651-616). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurobindo Pharma Limited, 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

Package Label-principal Display Panel (200 mg (120 Tablets Bottle))

Package Label-principal Display Panel (200 mg (120 Tablets Bottle))
Rufinamide Tablets, USP 200 mg film-coated tablets label from Aurobindo Pharma Limited. The label states each tablet contains Rufinamide USP 200 mg and the package contains 120 tablets. It includes storage instructions, distributor information (Aurobindo Pharma USA, Inc.), and a barcode. The label also highlights the requirement to dispense a Medication Guide with each product.*
FDA Label Image

Package Label-principal Display Panel (400 mg (120 Tablets Bottle))

Package Label-principal Display Panel (400 mg (120 Tablets Bottle))
Label for Rufinamide Tablets USP 400 mg film-coated oral tablets. The label indicates a quantity of 120 tablets, distributed by Aurobindo Pharma USA, Inc. It includes storage instructions, a medication guide warning, and a barcode. The label shows the manufacturer as Aurobindo Pharma Limited, with the product made in India.*
FDA Label Image

Str (Rufinamide Str)

Str (Rufinamide Str)
Chemical structure diagram of rufinamide, depicting its molecular layout with two fluorine atoms attached to a benzene ring linked to a triazole ring containing nitrogen atoms, and an amide group present on the triazole ring.*

* 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.