Supernus Pharmaceuticals, Inc. recalls Trokendi XR (topiramate) extended-release capsule, 50mg, 30-count blister pack, Rx only, Manufactured by: Catalent Pharm
Recalled October 26, 2016 · FDA recall D-0112-2017 · Supernus Pharmaceuticals
Hazard
Superpotent Drug: Failure of assay specifications in the capsule. · FDA Class II
Units
17,128 (30-count blister packs)
Sold at
Nationwide
Description
Superpotent Drug: Failure of assay specifications in the capsule.
Product
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
Manufacturer(s)
Supernus Pharmaceuticals, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →