Phenytoin Sodium Capsule, Extended Release
Product Images NDC 62756-299

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 Phenytoin Sodium (NDC 62756-299). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Pharmaceutical Industries, 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

Chemical Structure
Chemical structure of phenytoin sodium showing the molecular arrangement and bonding of its atoms as depicted in the image.*
FDA Label Image

Phenytoin-label-200mg (Phenytoin Label 200mg)

Phenytoin-label-200mg (Phenytoin Label 200mg)
Label for Extended Phenytoin Sodium Capsules USP, 200 mg, by Sun Pharmaceutical Industries, Inc. The label includes dosage form as extended-release capsules, quantity of 30 capsules, and storage instructions. It shows the NDC 62756-299-83 and distribution and manufacturing details including locations in New Jersey, USA, and Gujarat, India. The label also contains pharmacist dispensing instructions and a medication guide URL.*
FDA Label Image

Phenytoin-label-300mg (Phenytoin Label 300mg)

Phenytoin-label-300mg (Phenytoin Label 300mg)
Label for Extended Phenytoin Sodium Capsules USP, 300 mg, extended-release oral capsules. The product contains 30 capsules per container, labeled for prescription use only. Distributed by Sun Pharmaceutical Industries, Inc., Cranbury, NJ, and manufactured by Sun Pharmaceutical Industries Limited, Halol-Baroda Highway, Gujarat, India. Storage and handling instructions are included.*

* 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.