Nuvigil
Product Images NDC 42254-014

3 FDA label images from Rebel Distributors Corp · 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 Nuvigil (NDC 42254-014). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rebel Distributors Corp, 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

Chemical Structure (10f918f7 4782 470e A50e 35c7c66bfd79 01)

Chemical Structure (10f918f7 4782 470e A50e 35c7c66bfd79 01)
Chemical structure of the active ingredient in Nuvigil, showing a sulfoxide linked to two phenyl groups and an amide functional group typical of armodafinil.*
FDA Label Image

Warning Box For mg (10f918f7 4782 470e A50e 35c7c66bfd79 02)

Warning Box For mg (10f918f7 4782 470e A50e 35c7c66bfd79 02)
This text panel provides a warning that Nuvigil is a federally controlled substance (C-IV) due to potential abuse and dependence. It advises keeping Nuvigil secure to prevent misuse and states that selling or giving it away is illegal. It also recommends informing a doctor about any history of substance dependence or abuse.*
FDA Label Image

Nuvigil 50mg (10f918f7 4782 470e A50e 35c7c66bfd79 03)

Nuvigil 50mg (10f918f7 4782 470e A50e 35c7c66bfd79 03)
Nuvigil 50 mg tablets packaging label from Rebel Distributors Corp, containing 30 tablets. The label states each tablet contains 50 mg of Armodafinil. It includes identification details such as the NDC (42254-014-30), lot number, expiration date, and storage instructions. Distributed by Physician Partner, Thousand Oaks, CA.*

* 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.