Topiramate Capsule, Coated Pellets
Product Images NDC 65841-652

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Topiramate (NDC 65841-652). 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

Topiramate Capsules (sprinkle), 15 mg (C45924d5 C45b 4f31 Afa5 0cbc090d2816 01)

Topiramate Capsules USP 15 mg coated pellets packaged by Zydus Lifesciences Limited. The label states each capsule contains 15 mg of topiramate. The package includes 60 capsules with instructions for pharmacists to dispense a Medication Guide separately. Storage is recommended at 20° to 25°C, with warnings to protect from moisture and keep out of children's reach. Manufacturer details and contact for the Medication Guide are also provided.*

FDA Label Image

Topiramate Capsules (sprinkle), 25 mg (C45924d5 C45b 4f31 Afa5 0cbc090d2816 02)

Label for Topiramate Capsules, USP 25 mg by Zydus Lifesciences Limited. The label details packaging for 60 coated pellet capsules, with instructions to dispense the medication guide to patients. It includes storage instructions, dosage reference, and contact information for the medication guide, emphasizing keeping out of reach of children.*

FDA Label Image

50 mg Label (C45924d5 C45b 4f31 Afa5 0cbc090d2816 03)

Topiramate Capsules, USP 50 mg, oral coated pellets in a bottle label by Zydus Lifesciences Limited. The label indicates the package contains 60 capsules. It includes storage instructions, dosing guidance to see package insert, child-resistant packaging notice, and pharmacist medication guide dispensing information.*

* 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.