Zonisamide Capsule
Product Images NDC 80425-0370

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Zonisamide (NDC 80425-0370). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Advanced Rx 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

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FDA Label Image

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Chemical structure of zonisamide, depicting its molecular arrangement with a benzisoxazole ring and a sulfonamide functional group.*
FDA Label Image

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A cumulative percentage plot showing the percent reduction in all partial seizures rate comparing Zonisamide (blue line) and Placebo (red line) across a decreasing percentage of patients. The y-axis measures percent reduction in seizure rate, with improvement upwards and worsening downwards. The x-axis represents the percent of patients, decreasing from 100 to 0. The chart visualizes seizure reduction efficacy between the Zonisamide and placebo treatment arms.*
FDA Label Image

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FDA Label Image

Zonisamide 100mg Capsules #30 (Zonisamide 100mg Capsules 80425 0370 01)

Zonisamide 100mg Capsules #30 (Zonisamide 100mg Capsules 80425 0370 01)
Zonisamide 100 mg oral capsules packaging label by Advanced Rx of Tennessee, LLC. The label includes a green and yellow color scheme, with storage instructions (20°-25°C) and a caution to keep the medication out of reach of children. It lists the product NDC (80425-0370) and compares to ZONEGRAN with a source NDC 29300-0430-01. The label indicates prescription use (Rx Only) and an expiration date of 12/4/2023.*

* 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.