FDAFDA · Food and drugs·Recall number D-0112-2017
Trokendi XR (topiramate) extended-release capsule, 50mg, 30-count blister pack, Rx only, Manufactured by: Catalent Pharma Solutions, Winchester, KY 40391, Manufactured for: Supernus Pharmaceuticals, Inc., Rockville, MD 20850, NDC 17772-102-15
Published October 26, 2016 · Recall initiated: July 12, 2016
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Superpotent Drug: Failure of assay specifications in the capsule.
What to do
Voluntary: Firm initiated · E-Mail
Recall details
- Brand
- TROKENDI XR
- Manufacturer
- Supernus Pharmaceuticals, Inc.
- Distributor
- Nationwide
- UPC
- 0317772101300
- Lot
- Lot # 426636, Exp 4/22/18
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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