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
- Check the lot number and expiry on your medicine against the recall above.
- Talk to your pharmacist or doctor before changing anything — don't stop on your own.
- 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
| Distributed by / for | Supernus Pharmaceuticals, Inc., Rockville, MD 20850 USA |
| NDC | 17772-101-30 |
Show the full FDA record
| Full product label | 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. |
| Recalling firm | Supernus Pharmaceuticals, Inc. |
| Distribution | US Nationwide. |
| Quantity | 15,853 bottles |
| Recall initiated | 2026-07-06 |
| Report date | 2026-07-29 |
| Recall completed | — |
| Recall number | D-0758-2026 |
| Classification | Class III |
| FDA status | Ongoing |
| Origin on file | Rockville MD United States |
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.