Extended Phenytoin Sodium Capsule
Product Images NDC 65862-692

3 FDA label images from Aurobindo Pharma Limited · 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 Extended Phenytoin Sodium (NDC 65862-692). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurobindo Pharma Limited, 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

Package Label-principal Display Panel (100 mg (100 Capsules))

Package Label-principal Display Panel (100 mg (100 Capsules))
Label for Extended Phenytoin Sodium Capsules USP, 100 mg strength, containing 100 capsules. The label states the active ingredient as Phenytoin sodium USP 100 mg per capsule and includes storage instructions and a pharmacist dispensing note. Distributed by Aurobindo Pharma USA, Inc., made in India.*
FDA Label Image

Package Label-principal Display Panel (100 mg (10 x 10 Unit dose Capsules))

Package Label-principal Display Panel (100 mg (10 x 10 Unit dose Capsules))
Packaging label for Extended Phenytoin Sodium Capsules USP 100 mg by Aurobindo Pharma Limited. The carton shows a 100-count supply of unit-dose capsules, marked as Rx only. The label includes storage instructions, pharmacist notes, and distributor information for Aurobindo Pharma USA, Inc.*
FDA Label Image

Chemical Structure (Phenytoin Str)

Chemical Structure (Phenytoin Str)
Chemical structure of phenytoin sodium, showing the molecular framework with two phenyl rings, an imide group, and other ring features consistent with the active ingredient phenytoin sodium.*

* 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.