Topiramate Tablet
Product Images NDC 63187-758

3 FDA label images from Proficient Rx Lp · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Topiramate (NDC 63187-758). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Proficient Rx Lp, 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

Topi (40ba980b 018b 4973 91e5 Ec57c21fdc12 01)

Topi (40ba980b 018b 4973 91e5 Ec57c21fdc12 01)
Chemical structure diagram of the active ingredient Topiramate. The structure shows a complex arrangement of rings and functional groups, including methanesulfonamide and ether components, characteristic of Topiramate.*
FDA Label Image

Topi (40ba980b 018b 4973 91e5 Ec57c21fdc12 02)

Topi (40ba980b 018b 4973 91e5 Ec57c21fdc12 02)
A cumulative rate plot for time to an event, showing two curves with one generally higher than the other. The vertical axis is labeled 'Cumulative Rates for Time to' and the horizontal axis is marked with numerical increments up to 450. A p-value of 0.0002 is displayed on the graph, indicating statistical significance.*
FDA Label Image

Image 01

Image 01
Topiramate 50 mg tablets packaging label from Proficient Rx LP. The label indicates 90 tablets per container, with instructions to dispense the enclosed Medication Guide. Each film-coated tablet contains 50 mg of Topiramate USP. Tablets are described as light orange, circular, biconvex, and debossed with '123' on one side and 'C' on the other. Manufactured by Cipla Ltd., Kurkumbh, India, with storage instructions at 20°-25°C (68°-77°F).*

* 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.