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Class III · Lower riskActive recall

Trokendi Xr

Unlikely to cause harm — often a labeling or packaging issue.

Does this affect you?
Check your lot numberLot # 2075801, Exp Date: 31-Oct-2029.
Where it was soldUS Nationwide.
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.

What happened

Failed Dissolution Specifications

What to do

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Made byCatalent Pharma Solutions, Winchester, KY 40391 USA, Manufactured for: Supernus Pharmaceuticals, Inc., Rockville, MD 20850 USA
Brand nameTROKENDI XR
Generic nameTOPIRAMATE
Active ingredient(s)TOPIRAMATE
Distributed by / forSupernus Pharmaceuticals, Inc., Rockville, MD 20850 USA
NDC17772-101-30
Show the full FDA record
Full product labelTrokendi 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.
Recalling firmSupernus Pharmaceuticals, Inc.
DistributionUS Nationwide.
Quantity15,853 bottles
Recall initiated2026-07-06
Report date2026-07-29
Recall completed—
Recall numberD-0758-2026
ClassificationClass III
FDA statusOngoing
Origin on fileRockville MD United States

Related

Recent drug recallsCheck another medication

Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗

This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.