Topiramate Tablet
Product Images NDC 68071-3088

3 FDA label images from Nucare Pharmaceuticals, Inc. · 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 68071-3088). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Nucare Pharmaceuticals, Inc., 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 Topiramate, showing its molecular arrangement including carbon, oxygen, sulfur, nitrogen, and hydrogen atoms as represented by standard chemical notation.*
FDA Label Image

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

Topi (40ba980b 018b 4973 91e5 Ec57c21fdc12 02)
A cumulative rate graph showing two lines comparing time to an event, with the y-axis labeled 'Cumulative Rates for Time to' and a p-value of 0.0002 indicated on the graph. The x-axis extends to at least 450 units, likely days or similar measure, and the y-axis ranges up to 0.35, illustrating the difference between two comparative data sets over time.*
FDA Label Image

68071 3088 3

68071 3088 3
Topiramate 100 mg tablets packaging label from NuCare Pharmaceuticals, Inc. The label shows a bottle containing 30 film-coated oral tablets, each containing Topiramate USP 100 mg. The label includes NDC 68071-3088-3 and product number P1813030, instructions to keep out of reach of children, storage temperature guidelines, and manufacturer information identifying Cipla Ltd. Kurkumbh, India.*

* 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.