Modafinil Tablet
Product Images NDC 0904-6791

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Modafinil (NDC 0904-6791). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Major Pharmaceuticals, 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

A2501635 6969 Cca6 92c1 E6259d7d7708 00

Modafinil 200 mg tablets, USP, oral dosage form by Major Pharmaceuticals. The label displays the product name, strength, NDC 0904-6792-04, and indicates it is a Unit Dose pack containing 30 tablets. It includes usage instructions stating the medication is prescription-only and includes storage and safety information.*

FDA Label Image

A2501635 6969 Cca6 92c1 E6259d7d7708 01

Packaging label for Modafinil tablets, USP 100 mg, oral tablets by Major Pharmaceuticals. The label indicates the unit dose packaging containing 30 tablets, prescription only, with pharmacist dispensing instructions and storage conditions. The label also includes NDC numbers 0904-6791-04 and 0904-6791-04, and distribution information for Major Pharmaceuticals in Weston, Florida.*

FDA Label Image

Modafinil-01.jpg (Modafinil 01)

Chemical structure of modafinil, showing its molecular arrangement including two phenyl rings, a sulfinyl group, and an amide functional group.*

FDA Label Image

Modafinil-02.jpg (Modafinil 02)

Modafinil 200 mg oral tablets packaging label by Major Pharmaceuticals. The label features the proprietary name Modafinil and generic name modafinil. The label design includes a black and white color scheme with the labeler name prominently displayed.*

* 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.