Modafinil Tablet
Product Images NDC 65862-601

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 Modafinil (NDC 65862-601). 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 (100 mg (100 Tablets Bottle))

Package Label-principal Display Panel (100 mg (100 Tablets Bottle))
Label for Modafinil Tablets USP 100 mg by Aurobindo Pharma Limited, indicating an Rx-only drug. The label states the package contains 100 tablets, each with 100 mg of Modafinil. It includes storage instructions and distributor information for Aurobindo Pharma USA, Inc., with product origin listed as India. The label also features dosage details and prescription guidance.*
FDA Label Image

Package Label-principal Display Panel (200 mg (100 Tablets Bottle))

Package Label-principal Display Panel (200 mg (100 Tablets Bottle))
Label for Modafinil Tablets USP 200 mg by Aurobindo Pharma Limited. The label indicates 100 tablets per package and includes storage instructions (20° to 25°C), dispensing advice, distributor information (Aurobindo Pharma USA, Inc., New Jersey), and notes that the product is made in India. The label features an NDC code 65862-602-01 and a barcode.*
FDA Label Image

Chemical Structure (Modafinil Str)

Chemical Structure (Modafinil Str)
Chemical structure of Modafinil, showing a sulfinylacetamide core with diphenyl groups attached to the sulfur atom and an amide group at the terminal end.*

* 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.