Topiramate Tablet, Film Coated
Product Images NDC 80425-0092

4 FDA label images from Advanced Rx Pharmacy Of Tennessee, Llc · 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 80425-0092). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Advanced Rx Pharmacy Of Tennessee, Llc, 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

Fig 1

Fig 1
A line graph showing cumulative rates for time to first seizure over 500 days for Topiramate at doses 50 mg/day (solid line) and 400 mg/day (dashed line), with sample sizes of 234 and 236 respectively. The graph illustrates seizure occurrence over time with statistical significance (P = 0.0002).*
FDA Label Image

Fig 2

Fig 2
A bar chart showing change from baseline to double-blind phase in average monthly migraine period rate (±SE) across placebo and three Topiramate daily doses: 50 mg, 100 mg, and 200 mg. Data from Studies 11 and 12 is compared, with numbers of participants noted for each group. Statistical significance is indicated for 100 mg and 200 mg doses.*
FDA Label Image

Structure

Structure
Chemical structure of Topiramate, showing its specific arrangement of atoms and functional groups as depicted in the molecular diagram.*
FDA Label Image

Topiramate 50mg Tab Qty 60 Ndc 80425 0092

Topiramate 50mg Tab Qty 60 Ndc 80425 0092
Topiramate 50 mg tablet film-coated bottle label from Advanced Rx Pharmacy of Tennessee, LLC. The label indicates a 60-count package with NDC 80425-0092-02 and references Zydus Pharmaceuical source. Storage instructions specify room temperature 20°-25°C (68°-77°F).*

* 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.