Topiramate
Product Images NDC 68258-7159

3 FDA label images from Dispensing Solutions, 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 Topiramate (NDC 68258-7159). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Dispensing Solutions, 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

Ndc 68258-7159-xx (Ndc 68258 7159 Xx Caraco)

Ndc 68258-7159-xx (Ndc 68258 7159 Xx      Caraco)
Packaging label for Topiramate 200 mg tablets by Dispensing Solutions, Inc. The label features dosage information, NDC 68258-7159-XX, and warnings including use caution if operating machinery and risks during pregnancy. The label includes distributor details from Caraco Pharmaceutical Laboratories and storage instructions at 68°-77°F. It is marked RX only with sample lot and expiration placeholders.*
FDA Label Image

Topiramate-fig01 (Topiramate Fig01)

Topiramate-fig01 (Topiramate Fig01)
A line graph showing cumulative rates of time to first seizure over 500 days comparing Topiramate 50 mg/day and 400 mg/day doses. The x-axis represents time in days, and the y-axis shows cumulative rates. Two curves depict seizure occurrence rates for the two dosage groups, with a p-value of 0.0002 indicating statistical comparison.*
FDA Label Image

Topiramate-structure (Topiramate Structure)

Topiramate-structure (Topiramate Structure)
Chemical structure of the active ingredient Topiramate, showing its molecular framework including oxygen, carbon, sulfur, nitrogen, and hydrogen atoms arranged in a bicyclic configuration.*

* 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.