Modafinil Tablet
Product Images NDC 87063-308

3 FDA label images from Asclemed Usa Inc. · 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 Modafinil (NDC 87063-308). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Asclemed Usa 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.

Product Images & Figures Index

FDA Label Image

Modafinil Tablets Usp, 100mg And 200mg (452d2687 49ff 4734 8799 A4a5264cc584 01)

Modafinil Tablets Usp, 100mg And 200mg (452d2687 49ff 4734 8799 A4a5264cc584 01)
Chemical structure of Modafinil showing its molecular arrangement including a sulfinyl group linked to a diphenylmethyl and an acetamide moiety.*
FDA Label Image

100 (Label 100mg)

100 (Label 100mg)
Labels for Modafinil Tablets, USP 100 mg by Enovachem Pharmaceuticals, including relabeled and packaged versions. The labels display the product name, strength, NDC codes (87063-308 series), quantity options of 30, 60, 90, and 100 tablets, and directions to store at controlled room temperature. They also include the distributor Viona Pharmaceuticals Inc., Drug Enforcement Administration schedule (CIV), and caution statements about prescription-only dispensing.*
FDA Label Image

200 (Label 200mg)

200 (Label 200mg)
Modafinil Tablets, USP 200 mg oral tablets packaging labels by Enovachem Pharmaceuticals. Labels indicate quantities of 30, 60, 90, and 100 tablets, with NDCs 87063-309-30 through 87063-309-01. Distributed by Viona Pharmaceuticals Inc., each label includes storage instructions, a federal warning, and a barcode.*

* 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.