Topiramate
Product Images NDC 53808-0932

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Topiramate (NDC 53808-0932). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by State Of Florida Doh Central Pharmacy, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Graph (Topiramate F1)

Graph (Topiramate F1)
A line graph showing cumulative rates for 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 the cumulative rate. Two lines are plotted: a solid line for 50 mg/day and a dotted line for 400 mg/day, with a p-value of 0.0002 indicated.*
FDA Label Image

Display (Topiramate F2)

Display (Topiramate F2)
Topiramate tablets imprinted with the number 93 on one side and various four-digit codes on the other side, including 155, 7540, 7219, and 7220. The image shows four individual gray, capsule-shaped tablets with these imprints. The labeler is State of Florida DOH Central Pharmacy.*
FDA Label Image

Formula (Topiramate S)

Formula (Topiramate S)
Chemical structure of Topiramate showing its molecular framework with multiple ring systems, functional groups including a sulfate group, and methyl substituents.*
FDA Label Image

Label (Topiramate25mg(teva))

Label (Topiramate25mg(teva))
Topiramate 25 mg tablets packaging label showing a quantity of 30 tablets. The label includes lot number 28T015, expiration date 06/3010, and indicates packaging by DOH Central Pharmacy, Tallahassee, FL. A barcode with UPC 300930155109 is also visible.*

* 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.