Topiramate Tablet, Film Coated
Product Images NDC 71335-1116

4 FDA label images from Bryant Ranch Prepack · 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 71335-1116). 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

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39703b05 F774 4aed 9792 000a61531553 01
Chemical structure diagram of the active ingredient topiramate, showing its molecular arrangement with rings, oxygen atoms, and methyl groups.*
FDA Label Image

39703b05 F774 4aed 9792 000a61531553 02

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A Kaplan-Meier curve graph showing cumulative rates for time to first seizure over approximately 500 days comparing topiramate 50 mg/day and 400 mg/day doses. The solid line represents 50 mg/day (N=234) and the dashed line represents 400 mg/day (N=236). The graph indicates a statistically significant difference (P = 0.0002) in seizure occurrence over time between the two dosage groups.*
FDA Label Image

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A bar chart depicting the change from baseline to double-blind phase in average monthly migraine period rate (+SE) for placebo and topiramate at 50 mg/day, 100 mg/day, and 200 mg/day doses across two studies (Study 11 and Study 12). The chart shows reductions in migraine rate with increasing topiramate doses compared to placebo, with statistical significance indicated for the 100 mg/day and 200 mg/day doses.*
FDA Label Image

Label Image (Lbl713351116)

Label Image (Lbl713351116)
Topiramate 200 mg film-coated tablet packaging label by Bryant Ranch Prepack, indicating comparison to Topamax 200 mg tablet by Cadila Healthcare Ltd. The label shows storage instructions at 20°-25°C (68°-77°F) and a barcode with NDC 71335-1116. The package contains 30 tablets and is designated Rx only.*

* 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.