FDA · Drugs ·
Trokendi XR, topiramate extended-release capsules recall
Supernus Pharmaceuticals, Inc. recalled Trokendi XR, topiramate extended-release capsules on July 29, 2026 because of failed dissolution specifications. It was sold nationwide.
Why it was recalled
Failed Dissolution Specifications
What's recalled
Trokendi XR, topiramate extended-release capsules, 25mg, 30 Capsules, Rx only, Manufactured by: Catalent Pharma Solutions, Winchester, KY 40391 USA, Manufactured for: Supernus Pharmaceuticals, Inc., Rockville, MD 20850 USA, NDC 17772-101-30.
Quantity: 15,853 bottles
What to do
Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.
Read the official FDA noticeDetails
- Company
- Supernus Pharmaceuticals, Inc., Rockville, MD
- Date
- Severity
- Class III
the product is unlikely to cause health problems but breaks a rule. - Where sold
- Nationwide
US Nationwide. - Status
- Ongoing
- Recall number
- D-0758-2026
- Source
- U.S. Food and Drug Administration
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