Armodafinil Tablet
Product Images NDC 69339-178

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Armodafinil (NDC 69339-178). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Natco Pharma 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

Structure (Armodafinil Tablets Structure)

Chemical structure of Armodafinil, showing two phenyl rings attached to a sulfinyl group linked to an acetamide moiety.*

FDA Label Image

Bottle-label (Armodafinil 50mg 30s)

Armodafinil 50 mg oral tablets label from Natco Pharma USA LLC. The package contains 30 tablets. The label includes storage instructions, dispensing guidance, manufacturer details for Natco Pharma Limited, India, and mention of Natco Pharma USA LLC in New Jersey as the manufacturer for distribution.*

FDA Label Image

Bottle-label (Armodafinil 50mg 1000s)

Armodafinil Tablets 50 mg oral tablets package label from Natco Pharma USA LLC. The label indicates 1000 tablets in the package, with storage instructions between 20°-25°C (68°-77°F). It includes a barcode and states the product is prescription only (Rx only). The label also mentions manufacturing by Natco Pharma Limited, India, and manufacturing for Natco Pharma USA LLC in New Jersey, USA.*

FDA Label Image

Bottle-label (Armodafinil 150mg 30s)

Packaging label for Armodafinil Tablets 150 mg by Natco Pharma USA LLC. The label indicates a package of 30 oral tablets with prescription-only status, displaying the NDC number 69339-178-03. The label includes storage instructions, manufacturing details, and a barcode.*

FDA Label Image

Bottle-label (Armodafinil 150mg 1000s)

Label for Armodafinil Tablets 150 mg, oral dosage form, by Natco Pharma USA LLC. The label states the package contains 1000 tablets, prescription only, with storage instructions at 20°-25°C (68°-77°F). It includes directions to dispense with an accompanying Medication Guide and manufacturing details for Natco Pharma Limited, India, and Natco Pharma USA LLC, Parsippany, NJ.*

FDA Label Image

Bottle-label (Armodafinil 200mg 30s)

Label for Armodafinil Tablets 200 mg by Natco Pharma USA LLC. The label indicates a package size of 30 tablets, with prescription only status. The label includes storage instructions at 20°-25°C and manufacturer details for Natco Pharma Limited, India, and Natco Pharma USA LLC, Parsippany, NJ. It features a barcode and NDC 69339-179-03.*

FDA Label Image

Bottle-label (Armodafinil 200mg 1000s)

Armodafinil Tablets 200 mg oral tablet packaging label showing 1000 tablets. The label includes the NDC 69339-179-10, Rx only status, and instructions to store at 20°-25°C. Manufactured by Natco Pharma Limited, India, for Natco Pharma USA LLC, Parsippany, NJ. The label also displays the Natco Pharma USA logo and a barcode.*

FDA Label Image

Bottle-label (Armodafinil 250mg 30s)

Armodafinil Tablets 250 mg oral tablets in a pack of 30, labeled for prescription use only. The packaging displays the National Drug Code (NDC) 69339-180-03 and states it is manufactured by Natco Pharma Limited, India, for Natco Pharma USA LLC. The label instructs pharmacists to dispense the accompanying Medication Guide to each patient and includes storage instructions at 20°-25°C (68°-77°F).*

FDA Label Image

Bottle-label (Armodafinil 250mg 500s)

Label for Armodafinil Tablets 250 mg by Natco Pharma USA LLC showing a quantity of 500 tablets. The label includes the NDC 69339-180-05, dosage strength, Rx only status, storage instructions (20°-25°C), and manufacturer information for Natco Pharma Limited, India. The packaging also features a barcode and pill image with imprint 'NYC 375.'*

* 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.