Topiramate Tablet, Film Coated
Product Images NDC 72162-2481

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 72162-2481). 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 diagram of topiramate, showing its molecular bonds and atomic composition.*
FDA Label Image

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A Kaplan-Meier cumulative incidence curve chart showing time to first seizure for patients treated with Topiramate 50 mg/day and 400 mg/day. The x-axis represents time in days up to 500, and the y-axis shows cumulative rates for time to first seizure. The chart compares seizure onset rates between the two dosage groups with a p-value of 0.0002 indicating statistical significance.*
FDA Label Image

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A bar graph showing the change from baseline to double-blind phase in average monthly migraine period rate for placebo and topiramate doses (50 mg/day, 100 mg/day, 200 mg/day) across two studies. The graph includes error bars representing standard error and indicates statistical significance with asterisks for various topiramate doses compared to placebo.*
FDA Label Image

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FDA Label Image

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Label for Topiramate Tablets, USP 50 mg film-coated tablets, oral use, packaged as 60 tablets. The label indicates repackaging by Bryant Ranch Prepack, Inc., Burbank, CA, and manufacturing by Unichem Laboratories Ltd. It includes storage instructions, a barcode, NDC 72162-2481, and QR codes for product literature 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.