Extended Phenytoin Sodium
Product Images NDC 55648-720

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 Extended Phenytoin Sodium (NDC 55648-720). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Wockhardt 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

Structure (Extendedphenytoin M Figure 01)

Structure (Extendedphenytoin M Figure 01)
Chemical structure of phenytoin sodium, the active ingredient of EXTENDED PHENYTOIN SODIUM by Wockhardt Limited. The structure includes two phenyl rings attached to a hydantoin skeleton with a sodium ion.*
FDA Label Image

Figure 01 (Extendedphenytoin M Figure 02)

Figure 01 (Extendedphenytoin M Figure 02)
Label for Extended Phenytoin Sodium Capsules, USP 100 mg by Wockhardt Limited. The label shows the quantity of 100 capsules, prescription-only status, storage instructions, and a barcode. It includes a note for pharmacists to dispense the enclosed Medication Guide and cautions not to dispense capsules with a color coat. Manufactured by Wockhardt Limited, Mumbai, India, and distributed by Wockhardt U.S. LLC, Parsippany, NJ.*
FDA Label Image

Figure02 (Extendedphenytoin M Figure 03)

Figure02 (Extendedphenytoin M Figure 03)
Extended Phenytoin Sodium Capsules, USP 100 mg by Wockhardt Limited. The label shows 1000 capsules in the container with dispensing instructions and storage conditions. It includes the product NDC 64679-720-02 and advises pharmacists to provide a Medication Guide. The label is primarily white with blue and red accents and lists manufacturer and distributor information.*

* 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.