Supernus Pharmaceuticals (SUPN) Receives Tentative FDA Approval
Get Alerts SUPN Hot Sheet
Join SI Premium – FREE
Supernus Pharmaceuticals, Inc. (Nasdaq: SUPN) received a tentative approval letter from the FDA for Trokendi XR™, a once-daily extended release formulation of topiramate (formerly known as SPN-538).
The letter states that the FDA completed its review of the Trokendi XR NDA and that no additional clinical trials are required. Our initial understanding is that final approval is conditioned on resolving a marketing exclusivity issue raised by the FDA regarding a specific pediatric population.
The letter states that the FDA completed its review of the Trokendi XR NDA and that no additional clinical trials are required. Our initial understanding is that final approval is conditioned on resolving a marketing exclusivity issue raised by the FDA regarding a specific pediatric population.
Serious News for Serious Traders! Try StreetInsider.com Premium Free!
You May Also Be Interested In
- FDA authorizes 11 ZYN Ultra nicotine pouches for Philip Morris
- Blue Star Gold reports phase 2 drilling results at Nutaaq target
- Ionis to present olezarsen and ION775 data at ESC Congress 2026
Create E-mail Alert Related Categories
FDA, Momentum MoversSign up for StreetInsider Free!
Receive full access to all new and archived articles, unlimited portfolio tracking, e-mail alerts, custom newswires and RSS feeds - and more!



Tweet
Share