Nuvigil
Product Images NDC 16590-345

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Nuvigil (NDC 16590-345). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Stat Rx Usa Llc, 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

Boxed Warning (6fbf9925 8349 4cfc A87b 58a269635bca 02)

A text panel warning that NUVIGIL is a federally controlled substance (C-IV) due to potential abuse and dependence. It advises keeping NUVIGIL safely to prevent misuse or abuse and states that selling or giving away the drug is illegal. It also recommends consulting a doctor if there is a history of abuse or dependence on alcohol, prescription medicines, or street drugs.*

FDA Label Image

Nuvigil C-iv 150 mg Label Image (Nuvigil C Iv 150 mg Label)

Nuvigil C-IV 150 mg tablet bottle label from STAT Rx USA LLC. The label states the product contains 30 tablets of Armodafinil 150 mg. It includes the NDC 16590-345-30 and manufacturer Cephalon, Inc., Frazer, PA. The label features dosage instructions, storage information, and a federal caution about prescription use.*

FDA Label Image

Nuvigil C-iv 250 mg Label Image (Nuvigil C Iv 250 mg Label)

Nuvigil C-IV 250 mg tablet packaging label from STAT Rx USA LLC, containing 30 tablets. The label identifies it as generic for Armodafinil 250 mg and includes the NDC 16590-394-30. Distributed by Cephalon, Inc. with relevant batch and expiration details.*

FDA Label Image

Chemical Structure (Nuvigil Structure)

Chemical structure of the active ingredient in NUVIGIL, showing a sulfoxide group linked to an amide and two phenyl rings.*

* 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.