Supernus Pharmaceuticals, Inc. recalls Trokendi XR, (topiramate) extended-release capsules, 50 mg,
See all recalls from Supernus Pharmaceuticals, Inc. →Recalled Product
Trokendi XR, (topiramate) extended-release capsules, 50 mg, 30 Capsules, Rx only, Manufactured by: Catalent Pharma Solutions, Winchester, KY 40391 USA, Manufactured for: Supernus Pharmaceuticals, Inc., Rockville, MD 20850 USA, NDC 17772-102-30.
Hazard / Issue
Failed dissolution specifications.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Lot# 2145283, Exp Date: 31-Mar-2030.
✅ What Should You Do?
- 1Stop taking this medication and contact your doctor or pharmacist immediately.
- 2Do NOT flush medications down the drain — use an FDA-approved drug take-back program.
- 3Check the lot number on your bottle or packaging against the recalled lots listed above.
- 4Report adverse events to FDA MedWatch or call 1-800-FDA-1088.
Looking for a safe alternative?
Search Amazon for Trokendi XR, (topiramate) extended-release →If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.
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