Zonisamide Capsule
Product Images NDC 70771-1143

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Zonisamide (NDC 70771-1143). 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

Zonisamide Capsules, 25 mg (A140305e 5978 48b1 8a43 3945ca59b2d0 03)

Zonisamide Capsules 25 mg oral capsules packaging label. The label shows the product name, strength (25 mg), quantity (100 capsules), Rx only, and manufacturer Zydus Lifesciences Limited. It includes storage instructions, a note to pharmacists to dispense the medication guide, and the NDC 70771-1142-1.*

FDA Label Image

Zonisamide Capsules, 50 mg (A140305e 5978 48b1 8a43 3945ca59b2d0 04)

Zonisamide 50 mg Capsules label showing 100 capsules in the package. The label includes dosage strength, NDC 70771-1143-1, and directions for pharmacists to dispense the Medication Guide. The manufacturer is Zydus Lifesciences Limited, with production by Cadila Healthcare Ltd., Ahmedabad, India. Storage instructions for 20° to 25°C in a dry, light-protected place are included.*

FDA Label Image

Zonisamide Capsules, 100 mg (A140305e 5978 48b1 8a43 3945ca59b2d0 05)

Zonisamide Capsules 100 mg oral dosage form in a 100 capsule package. The label includes NDC 70771-1144-1 and states that it is prescription only. It instructs pharmacists to dispense a medication guide with each patient. The product is manufactured by Cadila Healthcare Ltd., Ahmedabad, India, and labeled by Zydus Lifesciences Limited. Storage instructions and warnings are also 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.