Topiramate Capsule, Extended Release
Product Images NDC 70771-1317

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Topiramate (NDC 70771-1317). 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

763b3d7d B40e 4c42 A9da 9fa5a796150c 07

Packaging label for Topiramate Extended-Release Capsules, 25 mg strength, oral dosage form, in a 30-capsule bottle. The label shows the proprietary and generic name, dosing frequency (once daily), and manufacturer, Zydus Lifesciences Limited. It includes warnings to swallow whole and keep out of reach of children, along with storage instructions and a barcode.*

FDA Label Image

763b3d7d B40e 4c42 A9da 9fa5a796150c 08

Topiramate Extended-Release Capsules 50 mg label showing the product name, strength, and dosage form. The label includes instructions to swallow the capsule whole, storage conditions, and dispensing guidance. It states the package contains 30 capsules and is RX only. The label also names the manufacturer as Cadila Healthcare Ltd., located in Ahmedabad, India, and displays the Zydus Pharmaceuticals logo.*

FDA Label Image

763b3d7d B40e 4c42 A9da 9fa5a796150c 09

Label for Topiramate Extended-Release Capsules 100 mg by Zydus Lifesciences Limited, featuring a purple and orange design. The label states the product is oral capsules, provides a capsule image, indicates 30 capsules per container, and notes the drug is Rx only. It includes dosage storage instructions, manufacturer details, and barcode.*

* 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.