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Topiramate Tablet, Film Coated
Product Images NDC 68788-7568
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Topiramate (NDC 68788-7568). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Preferred Pharmaceuticals, 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.
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The text describes cumulative seizure rates for two different doses of Topiramate (50 mg/day and 400 mg/day) over time. There is a visual representation of this data on a graph with time in days on the x-axis and seizure rates on the y-axis. The graph shows that the higher dose of Topiramate resulted in a lower rate of seizures and the difference was statistically significant with a p-value of 0.0002.*
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The text describes the change in the average monthly migraine period rate during a double-blind phase in a study comparing Topiramate at different doses and Placebo. The data is presented in a table and indicates statistical significance (p<0.010 and p<0.001) for some of the treatment groups compared to Placebo.*
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This is a label of Topiramate Tablets, USP 200mg which is a generic drug for Topamax. The label warns that transferring the tablets is prohibited by Federal law. The tablets are manufactured by Zydus Pharmaceuticals USA Inc. and each film-coated tablet contains 200mg of topiramate. The rest of the information on the label pertains to lot numbers, expiration dates, and other manufacturing details.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.
