Topiramate Tablet, Film Coated
Product Images NDC 70518-2955

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Topiramate (NDC 70518-2955). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack 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

Figure1.jpg (Figure1)

FDA Label Image

Figure2.jpg (Figure2)

Figure2.jpg (Figure2)
The given text represents a table showing the change in the average monthly migraine period rate from baseline to the double-blind phase for four different groups, including a placebo and three different doses of Topiramate. The data is from two different studies, labeled as Study 10 and Study 11. The table also includes the sample sizes for each group and denotes the values that are statistically significant.*
FDA Label Image

Remedy_label (Remedy Label)

Remedy_label (Remedy Label)
Topiramate is a prescription medication package including thirty tablets identified as HD3. It is available only with a doctor's prescription, and the National Drug Code is 70518-2955-00. It is produced by Glenmark in Mahwah, NJ 07430, and repackaged by RemedyRepack Inc. in Indiana, PA 15701. The lot number and expiration date are not available, and storage instructions state to keep it within the range of 20°C to 26°C (63-77°F) with allowed excursions to 15-30°C (59-86°F) as per USP regulations. The package insert should be consulted for usage instruction, and this medication must be kept away from children.*
FDA Label Image

Structure.jpg (Structure)

FDA Label Image

Topiramate 100mg 70518 2955 01

Topiramate 100mg 70518 2955 01
Topiramate is a prescription medication that comes in a bottle labeled as HD3. The medication is only available with a doctor's prescription and should be kept out of the reach of children. It is manufactured by Glenmark in Mahwah, NJ and repackaged by RemedyRepack Inc. The NDC number for the medication is 70518-2955-01, and the source NDC is 68462-0109-60. The lot number and expiration date are not provided. The recommended storage temperature is 20-26°C (63-77°F), with excursions permitted to 15-30°C (59-86°F), as specified by USP. The package insert should be referred to for directions on how to use this medication.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.