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Topiramate Tablet, Film Coated
Product Images NDC 68788-8817
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Topiramate (NDC 68788-8817). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Preferred Pharmaceuticals 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.
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Chemical structure of topiramate, showing its molecular composition with various functional groups including sulfonamide and multiple methyl groups.*
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A cumulative rate graph depicting time to first seizure over 500 days for two dosing groups of topiramate: 50 mg/day and 400 mg/day, with sample sizes of 234 and 236 respectively. The y-axis represents cumulative rates, and the x-axis shows time in days. A p-value of 0.0002 is indicated on the graph.*
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A bar graph comparing changes from baseline to double-blind phase in average monthly migraine period rates for placebo and three doses of topiramate (50 mg/day, 100 mg/day, 200 mg/day) across two studies. The graph includes statistical significance indicators for dose-dependent migraine rate reductions with topiramate relative to placebo.*
Topiramate Tablets 25mg (9df497de Be9f 4244 A769 A72a0e64dc42 04)
Label for Topiramate Tablets 25 mg, a human prescription drug by Preferred Pharmaceuticals Inc. The label states the tablets are film-coated, contain 25 mg of topiramate, USP, and are generic for Topamax. It includes storage instructions, warnings about alcohol consumption, and dosing directions in English and Spanish. The manufacturer is Unichem Laboratories Ltd.*
* 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.
