Provigil Tablet
Product Images NDC 60429-010

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 Provigil (NDC 60429-010). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Golden State Medical Supply, Inc., 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

Provigil 100 mg (60429-009-30.jpg)

Provigil 100 mg (60429-009-30.jpg)
Label for Provigil 100 mg oral tablets containing modafinil, with a package count of 30 tablets. The label includes the NDC number 60429-009-30 and states that the medication requires a Medication Guide. The drug is marketed by GSMS, Incorporated and manufactured for Apotex Corp. Storage instructions specify 20°C to 25°C. Additional barcodes, lot, expiration, and serialization information areas are present.*
FDA Label Image

Provigil 200 mg (60429-010-30.jpg)

Provigil 200 mg (60429-010-30.jpg)
Provigil 200 mg oral tablets label showing a 30-tablet count. The label includes the generic name modafinil, mentions medication guide requirements, and storage instructions. It lists Apotex Corp. as manufacturer and GSMS, Incorporated as marketer. The label also features a barcode and a QR code area for lot, expiration, and serial number information.*
FDA Label Image

Chemical_image.jpg (Provigil Modafinil N020717 1)

Chemical_image.jpg (Provigil   Modafinil   N020717 1)
Chemical structure of modafinil, showing the molecular arrangement including benzene rings, sulfoxide group, and acetamide moiety, corresponding to the active ingredient in Provigil tablets.*

* 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.