Dilantin Capsule, Extended Release
Product Images NDC 70518-4325

View Photos of 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 Dilantin (NDC 70518-4325). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack 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

Mm2 (Dilantin 30mg 70518 4325 01)

Mm2 (Dilantin 30mg 70518 4325 01)
Label for Dilantin 30 mg extended phenytoin sodium capsule, extended release, with quantity of 1 capsule. The label includes instructions to protect from moisture and repackaging details from RemedyRepack Inc. It also mentions the original manufacturer as Viatris, Morgantown, WV, with storage instructions at 20-25°C. The label features the RemedyRepack logo and barcode.*
FDA Label Image

Remedy_label (Remedy Label)

Remedy_label (Remedy Label)
DILANTIN 30 mg extended release capsules label showing packaging details. The label indicates 100 capsules per box and includes reminders to protect from moisture. It is labeled for prescription use only, with NDC 70518-4325-00, manufactured by Viatris in Morgantown, WV, and repackaged by RemedyRepack Inc. The label includes storage instructions and a barcode with a QR code.*
FDA Label Image

Chemical Structure (Image 01)

Chemical Structure (Image 01)
Chemical structure diagram of extended phenytoin sodium, the active ingredient in DILANTIN capsules. The structure depicts the molecular arrangement characteristic of phenytoin sodium, corresponding to its pharmaceutical formulation.*

* 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.