Topiramate Tablet, Film Coated
Product Images NDC 72162-2483

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Topiramate (NDC 72162-2483). 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 formula with labeled atoms and bonds including oxygen, sulfur, nitrogen, carbon, and hydrogen groups in a detailed skeletal representation.*

FDA Label Image

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A cumulative incidence curve graph comparing time to first seizure for Topiramate 50 mg/day versus 400 mg/day. The x-axis represents time in days up to 500 days, and the y-axis shows cumulative rates for the first seizure. Two curves are shown, with Topiramate 400 mg/day having a lower cumulative seizure rate over time compared to 50 mg/day, including a statistical significance p-value of 0.0002.*

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 (± SE) for placebo and three doses of topiramate (50 mg/day, 100 mg/day, 200 mg/day) across two studies, showing greater reductions with higher doses of topiramate. Statistical significance is indicated for the 100 mg/day and 200 mg/day groups.*

FDA Label Image

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FDA Label Image

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Label for Topiramate Tablets, USP 200 mg film-coated tablets. The packaging indicates 60 tablets per container, repackaged by Bryant Ranch Prepack and manufactured by Unichem Laboratories Ltd. The label includes storage instructions, QR codes for product literature and medication guide, and cautions about prescription verification and moisture protection.*

* 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.