FDA Drug · D-0833-2026

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.

Class III · Ongoing

Failed dissolution specifications.

Advertisement
Advertisement
Affected lots / codes — check yours against thisLot# 2145283, Exp Date: 31-Mar-2030.
Recalling firm
Supernus Pharmaceuticals, Inc., Rockville, MD
Classification
Class III (unlikely to cause harm)
Status
Ongoing
Quantity
11304 bottles
Distribution
US Nationwide.
Recall initiated
August 31, 2026
Classified
September 3, 2026
Initiation
Voluntary: Firm initiated
Advertisement
Official source. This record is published by the U.S. FDA through the openFDA enforcement database. View the unmodified government record:
https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0833-2026%22
Advertisement
Important. Recalls target specific lots and codes — compare the affected lots above against your own product. This page reproduces public FDA data for readability; EveryRecall is independent and not affiliated with the FDA.
Check this brand across all 8 databases →