FDARecall 99767Medicines
What to do
The FDA record of this recall has no instruction for consumers. Compare the lot codes below with your product. If they match, do not use it, and follow the notice of the firm or ask the store where you bought it. Talk to your pharmacist or doctor before stopping a medicine.Note from Recalls Watch, not agency text.
Read the official notice on accessdata.fda.gov (opens in a new tab)
Hazard
Why it was recalled
Failed dissolution specifications.
FDA classification: Class III. Use is not likely to cause adverse health consequences. Status: Ongoing.
Is it yours? Products and codes
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.
- Lot or code
- Lot# 2145283, Exp Date: 31-Mar-2030.
- FDA recall number
- D-0833-2026
- Quantity
- 11304 bottles
Distribution (FDA): US Nationwide.
About this record
- Issued by
- U.S. Food and Drug Administration
- Firm
- Supernus Pharmaceuticals, Inc.
- Title
- Composed by Recalls Watch from fields of the record; FDA records have no title.