Topiramate Tablet, Film Coated
Product Images NDC 71335-0925

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 71335-0925). 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.

Product Images & Figures Index

FDA Label Image

Chemical-structure (Chemical Structure)

Chemical-structure (Chemical Structure)
Chemical structure of the active ingredient topiramate as shown in the image. The diagram depicts the molecular arrangement featuring multiple rings, ether groups, and sulfonamide functional groups characteristic of topiramate.*
FDA Label Image

Figure 1.jpg (Figure 1)

Figure 1.jpg (Figure 1)
A Kaplan-Meier survival curve graph showing cumulative rates for time to first seizure over 500 days for two dosages of Topiramate: 50 mg/day and 400 mg/day. The x-axis represents time in days, and the y-axis represents cumulative rates for time to first seizure. The graph compares seizure onset between the two dosage groups (N=234 and N=236) with a p-value of 0.0002 indicating statistical significance.*
FDA Label Image

Figure-2 (Figure 2)

Figure-2 (Figure 2)
A bar graph comparing the change from baseline to double-blind phase in average monthly migraine period rate for placebo and Topiramate at doses of 50 mg/day, 100 mg/day, and 200 mg/day. Data is shown for two studies, Study 11 and Study 12, with error bars representing standard error. Statistical significance markers indicate p-values less than 0.010 and 0.001 for higher doses.*
FDA Label Image

Label (Lbl713350925)

Label (Lbl713350925)
Topiramate Tablets, USP 200 mg product label showing a package of 30 tablets. Labeled as Rx only, repackaged by Bryant Ranch Prepack, Inc., Burbank, CA, and manufactured by Sun Pharmaceutical Industries Ltd. The label includes storage instructions and the product NDC 71335-0925-1 barcode.*

* 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.