Topiramate Tablet, Film Coated
Product Images NDC 65841-648

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Topiramate (NDC 65841-648). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Zydus Lifesciences Limited, 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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Topiramate Tablets USP 25 mg film-coated oral tablets packaging label. The label shows a count of 60 tablets, is marked Rx only, and includes storage and dosage advisory notes. Manufactured by Cadila Healthcare Ltd., Ahmedabad, India, with Zydus Pharmaceuticals branding.*

FDA Label Image

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Topiramate Tablets, USP 50 mg film-coated tablets packaging label by Zydus Lifesciences Limited. The label shows a white tablet with imprint 'ZD 15,' contains 60 tablets, and indicates prescription use only. The manufacturer is Cadila Healthcare Ltd., Ahmedabad, India.*

FDA Label Image

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Topiramate Tablets, USP 100 mg film-coated tablets packaged by Zydus Lifesciences Limited. The label shows a round white tablet imprinted with 'ZD 14'. The package contains 60 tablets for oral use, marked Rx only. It includes storage instructions, barcode, and manufacturer information from Cadila Healthcare Ltd., Ahmedabad, India.*

FDA Label Image

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Label for Topiramate Tablets USP 200 mg, film-coated oral tablets. The label includes a depiction of a round white tablet with imprint 'ZD 13'. It states the package contains 60 tablets and is for prescription use only, distributed by Zydus Pharmaceuticals. Storage and usage instructions are also included, with manufacturer Cadila Healthcare Ltd., Ahmedabad, India noted.*

* 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.