Supernus Pharmaceuticals, Inc.

FDA Regulatory Profile

Supernus Pharmaceuticals, Inc. appears in FDA public data with 2 recalls, 0 510(k) clearances, 6 FDA inspections, and 0 compliance actions on record. Its most recent recall (D-0758-2026, Class III) was initiated on July 6, 2026.

Summary

Total Recalls
2
510(k) Clearances
0
Inspections
6
Compliance Actions
0

Recent Recalls

NumberClassProductDate
D-0758-2026Class IIITrokendi XR, topiramate extended-release capsules, 25mg, 30 Capsules, Rx only, Manufactured by: CataJuly 6, 2026
D-0112-2017Class IITrokendi XR (topiramate) extended-release capsule, 50mg, 30-count blister pack, Rx only, ManufactureJuly 12, 2016