Topiramate
Product Images NDC 68258-3001

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Topiramate (NDC 68258-3001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Dispensing Solutions 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

Topiramate-label-100 mg (Ndc 68258 7056 01)

Label for TOPIRAMATE 100 mg tablets by Dispensing Solutions Inc. The white label includes product and manufacturer information, dosage form, and quantity of 60 tablets per container. It states the NDC number 68258-7056-06 and includes warnings about drowsiness and alcohol use, as well as storage temperature instructions. The label also features barcodes and a note that the product is prescription-only.*

FDA Label Image

Topiramate-label-25 mg (Ndc68258 3000 01)

TOPIRAMATE 25 mg tablet bottle label from Dispensing Solutions Inc. The label indicates 60 tablets per container and includes the NDC code 68258-3000-01. It states that each tablet contains 25 mg of topiramate USP and features a comparison note to Topamax. Additional information includes a warning to avoid alcohol and drowsiness caution, and instructions to take orally every specified hours.*

FDA Label Image

Topiramate-label-50 mg (Ndc68258 3001 01)

TOPIRAMATE 50 mg tablets packaging label from Dispensing Solutions Inc. The label shows 60 tablets, NDC 68258-3001-01, and Product # 7T0360. It includes dosage instructions to take orally every set hours, a warning about drowsiness, and advises caution for operating machinery or driving. The label also mentions storage instructions and sample lot information.*

FDA Label Image

Topiramate-label-200 mg (Ndc68258 3002 01)

TOPIRAMATE 200 mg tablet packaging label from Dispensing Solutions Inc. The label states the product contains 60 tablets, each with 200 mg of topiramate. It includes warnings, lot number, expiration date, and usage instructions. The label also shows the NDC number 68258-3002-01 and manufacturer Sun Pharmaceutical Industries Ltd.*

FDA Label Image

Topiramate-fig01 (Topiramate Fig01)

A line graph comparing the cumulative rates of time to first seizure for two dosages of Topiramate: 50 mg/day and 400 mg/day. The x-axis represents time in days (0 to 500), and the y-axis represents the cumulative rate to first seizure (0 to 0.5). The graph shows two curves for 234 and 236 subjects respectively, with a p-value of 0.0002 indicating statistical significance.*

FDA Label Image

Topiramate-structure (Topiramate Structure)

Chemical structure of the active ingredient Topiramate, showing its molecular arrangement with oxygen, sulfur, nitrogen, carbon, and hydrogen atoms in a cyclic configuration, including sulfonamide and isopropyl groups.*

* 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.