Topiramate Tablet, Film Coated
Product Images NDC 72162-2482

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Topiramate (NDC 72162-2482). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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

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Chemical structure of topiramate, depicting its molecular arrangement with labeled atoms and functional groups.*

FDA Label Image

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A line chart showing cumulative rates for time to first seizure comparing Topiramate 50 mg/day and 400 mg/day doses over a 500-day period. The x-axis represents time in days, and the y-axis shows cumulative seizure rates. Two lines illustrate different dosage groups with sample sizes noted as 234 and 236 patients, respectively.*

FDA Label Image

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A bar graph showing change from baseline to double-blind phase in average monthly migraine period rate (±SE) for two studies comparing placebo and topiramate at doses of 50 mg/day, 100 mg/day, and 200 mg/day. Bars represent Study 1 and Study 2 results, indicating greater reductions with increasing topiramate doses, with statistical significance indicated at p < 0.010 and p < 0.001 levels.*

FDA Label Image

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FDA Label Image

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Topiramate Tablets, USP 100 mg film-coated tablets label showing the product NDC 72162-2482-6, repackaged by Bryant Ranch Prepack, Inc. in Burbank, CA, and manufactured by Unichem Laboratories Ltd. The label indicates 60 tablets, with instructions to store at 20° to 25°C and protect from moisture. It includes QR codes for package insert and medication guide 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.