Topiramate Tablet, Film Coated
Product Images NDC 71335-0548

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Topiramate (NDC 71335-0548). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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

Chemical-structure (Chemical Structure)

FDA Label Image

Figure-1jpg (Figure 1)

FDA Label Image

Figure-2 (Figure 2)

FDA Label Image

Label (Lbl713350548)

Label (Lbl713350548)
This appears to be a medication label for Topiramate 25mg tablets, which are round and white in color, produced by Sun Pharmaceutical Industries Ltd. The manufacturer's instructions state that the medication should be stored in a tightly closed container at room temperature (20°-25°C, or 68°-77°F), with an expiration date of MM/YY (not provided in the text). The label also includes a National Drug Code (NDC) number (7133505481) and a unique product identifier (03994301523487), but no dosage instructions or other medical information is present.*

* 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.