Topiramate
Product Images NDC 64725-0710

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Topiramate (NDC 64725-0710). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Tya Pharmaceuticals, 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

Label Image (64725 0707)

Packaging label for Topiramate 25 mg tablets in a 60 count bottle. Label includes prescription-only status, lot number placeholder, expiration date placeholder, manufacturer as Sun Pharma, repackaged by TYA Pharmaceuticals in Tallahassee, FL, and a barcode. Directions to see the package insert for dosage information are also present.*

FDA Label Image

Label Image (64725 0710)

Label for TOPIRAMATE 50mg tablets, package size of 60 tablets. The label indicates the drug is Rx only, manufactured by SUN PHARMA and repackaged by TYA Pharmaceuticals at Tallahassee, FL. The label includes lot number, expiration date placeholders, a barcode, and directions to see package insert for dosing.*

FDA Label Image

Topiramate-fig01 (Topiramate Fig01)

A line graph showing cumulative rates for time to first seizure over time (days) for two dosing groups of Topiramate, 50 mg/day and 400 mg/day. The graph plots data points up to 500 days with distinct curves for each dosage, including sample sizes (N=234 and N=236) and a statistical significance value (p=0.0002).*

FDA Label Image

Topiramate-structure (Topiramate Structure)

Chemical structure of the active ingredient in TOPIRAMATE by TYA Pharmaceuticals, depicting the molecular arrangement including oxygen, sulfur, nitrogen, and carbon atoms.*

* 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.