Supernus Pharmaceuticals, Inc. Recall
Trokendi XR, (topiramate) extended-release capsules, 50 mg, 30 Capsules, Rx only, Manufactured by: Catalent Pharma Solutions, Winchester, KY
Updated August 31, 2026
Supernus Pharmaceuticals, Inc. is recalling Trokendi XR, (topiramate) extended-release capsules, 50 mg, 30 Capsules, Rx only, Manufactured by: Catalent Pharma Solutions, Winchester, KY. Hazard: Failed dissolution specifications.
Is the Supernus Pharmaceuticals, Inc. recalled? Yes. This product was recalled by FDA on August 31, 2026. Details below.
What is recalled
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.
Am I affected
You may be affected if you own this product. Check the brand, model, and lot/date codes listed in the recall against your item.
What to do right now
Voluntary: Firm initiated
The hazard
Failed dissolution specifications.
Brands affected
- Source
- FDA
- Category
- Drugs & Medications
- Recall ID
- fda-D-0833-2026
- Classification
- Class III
- Recalled
- August 31, 2026
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