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.

FDA Label Image

Chemical-structure (Chemical Structure)

FDA Label Image

Figure 1.jpg (Figure 1)

Figure 1.jpg (Figure 1)
This is a graph showing the cumulative rates for time to first seizure for two different doses of Topiramate (50mg/day and 400mg/day) over a period of 500 days. The graph also includes the percentage values (ranging from 0.00 to 0.50) on the y-axis and the time in days on the x-axis. The p-value for the comparison between the two doses is 0.0002.*
FDA Label Image

Figure-2 (Figure 2)

Figure-2 (Figure 2)
Not available. The given text does not provide enough information to generate a description.*
FDA Label Image

Label (Lbl713350925)

Label (Lbl713350925)
This is a description of a medication called "Topiramate Tablets, USP 200mg". Each tablet contains 200mg of Topiramate, and it should be stored in a tight, light-resistant container at room temperature. The medication comes in a bottle of 30 tablets, and it was repackaged by a company called Bryant Ranch Prepack, Inc. The manufacturer is Sun Pharmaceutical Industries Ltd. The NDC (National Drug Code) for this medication is 71335-0925-1.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.