Topiramate Tablet, Film Coated
Product Images NDC 72162-2480

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 72162-2480). 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, showing its molecular framework including oxygen atoms, methyl groups, and a sulfonamide moiety.*
FDA Label Image

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A line graph showing cumulative rates for time to first seizure over 500 days comparing two doses of topiramate, 50 mg/day and 400 mg/day, with respective sample sizes noted. The x-axis represents time in days, and the y-axis shows cumulative rates. A p-value of 0.0002 is indicated.*
FDA Label Image

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A bar chart comparing the change from baseline to double-blind phase in average monthly migraine period rate (± standard error) across four groups: placebo, topiramate 50 mg/day, 100 mg/day, and 200 mg/day. Two studies are represented by different bar patterns, showing a dose-dependent reduction in migraine rates with statistical significance indicated.*
FDA Label Image

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FDA Label Image

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Label for Topiramate Tablets, USP, 25 mg film-coated tablets. The label shows the product name, strength, package size of 60 tablets, and indicates it is Rx only. It lists Bryant Ranch Prepack as the labeler and Unichem Laboratories Ltd. as the manufacturer. Storage instructions and caution to protect from moisture are included. Two QR codes are visible for dosage information and medication guide.*

* 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.