Modafinil Tablet
Product Images NDC 69452-342

3 FDA label images from Bionpharma 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 69452-342). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bionpharma 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

Chemical Structure (Modafinil Tablets Figure 1)

Chemical Structure (Modafinil Tablets Figure 1)
Chemical structure of modafinil, displaying its molecular components including two phenyl rings, a sulfinyl group, and an amide group.*
FDA Label Image

Carton 100 mg 30s (Modafinil Tablets Figure 2)

Carton 100 mg 30s (Modafinil Tablets Figure 2)
Modafinil Tablets, USP 100 mg oral tablets carton by Bionpharma Inc. The label displays the strength as 100 mg and indicates a quantity of 30 tablets per package. It includes directions to dispense the medication guide separately and storage instructions at 20° to 25°C. The product is Rx only, made in India, and the label shows the NDC 69452-342-13 along with the manufacturer's address in Princeton, NJ.*
FDA Label Image

Carton 200 mg 30s (Modafinil Tablets Figure 3)

Carton 200 mg 30s (Modafinil Tablets Figure 3)
Modafinil Tablets, USP 200 mg oral tablets packaging label from Bionpharma Inc. The label shows the drug name, strength, quantity of 100 tablets, and storage instructions. It includes directions to dispense the Medication Guide separately and states the tablets contain 200 mg of modafinil. The distribution address in Princeton, NJ, and barcode are also visible.*

* 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.