Topiramate Tablet, Film Coated
Product Images NDC 70518-0233

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Topiramate (NDC 70518-0233). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack 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.

FDA Label Image

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Chemical structure diagram of topiramate, the active ingredient in the medication. The diagram shows the arrangement of atoms and bonds within the topiramate molecule, including multiple ring structures and functional groups.*

FDA Label Image

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A line graph comparing the cumulative rates for time to first seizure over a period of 500 days between two topiramate dosage groups: 50 mg/day and 400 mg/day. The graph shows cumulative seizure rates on the y-axis and time in days on the x-axis, with two lines representing the different dose groups, indicating lower seizure rates with the higher dose.*

FDA Label Image

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A bar chart showing change from baseline to double-blind phase in average monthly migraine period rate (±SE) for placebo and topiramate doses (50 mg/day, 100 mg/day, 200 mg/day) from two studies labeled Study 11 and Study 12. The x-axis lists the treatment groups and sample sizes; the y-axis shows the change rate with values from 0 to -3. Statistical significance markers indicate p < 0.010 and p < 0.001 for certain groups.*

FDA Label Image

Remedy_label (Remedy Label)

Label for topiramate 25 mg film-coated tablets by RemedyRepack Inc. The label states quantity of 30 tablets, oral route, RX only, NDC 70518-0233-00, and manufacturer Zydus Pharm, Pennington, NJ. It includes storage instructions and a QR code on a white background with purple accents.*

* 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.