Modafinil Tablet
Product Images NDC 71335-2258

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Modafinil (NDC 71335-2258). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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

Chem Structure (Chemstructure)

Chem Structure (Chemstructure)
Chemical structure diagram of Modafinil, showing its characteristic sulfinyl and amide functional groups attached to aromatic rings.*
FDA Label Image

Label (Lbl713352258)

Label (Lbl713352258)
Label for Modafinil Tablets USP, 200 mg oral tablets. The package contains 30 tablets, labeled for prescription use only. It is repackaged by Bryant Ranch Prepack, Inc., Burbank, CA, and manufactured by Sidmak Laboratories (India) Pvt. Ltd. The label includes storage instructions and a barcode.*
FDA Label Image

Modafinil-spl-tables (Modafini Spl Tables)

Modafinil-spl-tables (Modafini Spl Tables)
Two tables presenting clinical data for Modafinil tablets at 200 mg and 400 mg doses versus placebo. The first table shows average baseline sleep latency and changes at final visit measured by Maintenance of Wakefulness Test (MWT) and Multiple Sleep Latency Test (MSLT) across disorders including Narcolepsy I, Narcolepsy II, Obstructive Sleep Apnea (OSA), and Shift Work Disorder (SWD). The second table shows percent of patients who improved at final visit based on Clinical Global Impression of Change (CGI-C) for the same conditions and treatments.*
FDA Label Image

* 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.