Phenytek Capsule, Extended Release
Product Images NDC 0378-2670

3 FDA label images from Mylan Pharmaceuticals 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 Phenytek (NDC 0378-2670). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Mylan Pharmaceuticals 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

Phenytek Capsules 200 mg Bottle Label (Image 01)

Phenytek Capsules 200 mg Bottle Label (Image 01)
Label for Phenytek extended phenytoin sodium capsules, USP, 200 mg oral extended-release capsules by Mylan Pharmaceuticals Inc. The label states the dosage strength as 200 mg and the package contains 30 capsules. It includes usage instructions, storage information, and barcode details. The product is Rx only and manufactured for Mylan Pharmaceuticals in Morgantown, WV.*
FDA Label Image

Phenytek Capsules 300 mg Bottle Label (Image 02)

Phenytek Capsules 300 mg Bottle Label (Image 02)
Phenytek 300 mg extended phenytoin sodium capsules in an oral dosage form, packaged by Mylan Pharmaceuticals Inc. The label states each capsule contains 300 mg phenytoin sodium USP, available in a 30-capsule bottle. It includes pediatric dosage guidance, storage instructions for 20° to 25°C, and a requirement to keep the medication out of children's reach. The packaging shows a barcode, NDC 0378-3750-93, and labels the product as prescription only.*
FDA Label Image

Phenytoin Structural Formula (Image 03)

Phenytoin Structural Formula (Image 03)
Chemical structure of phenytoin sodium, the active ingredient in Phenytek extended release capsules.*

* 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.