Treats partial-onset seizures with or without secondarily generalized seizures. ANDA 218152, held by Msn. Perampanel.
As of Nov 14, 2026, ANDA 218152 (Perampanel), held by Msn, was first approved by FDA on Jul 11, 2025, with 0 approved supplements and 0 published complete response letters.
Perampanel, a non-competitive AMPA glutamate receptor antagonist, is indicated for: Treatment of partial-onset seizures with or without secondarily generalized seizures in patients with epilepsy 4 years of age and older Adjunctive therapy in the treatment of primary generalized tonic-clonic seizures in patients with epilepsy 12 years of age and older 1.1 Partial-Onset Seizures Perampanel oral suspension is indicated for the treatment of partial-onset seizures with or without secondarily generalized seizures in patients with epilepsy 4 years of age and older. 1.
| Date | Submission | Status | Documents |
|---|---|---|---|
| Jul 11, 2025 | Original application | Approved | None posted |
| Product | Active ingredient | Marketing |
|---|---|---|
| Perampanel0.5MG/ML · suspension;oral | Perampanel | Rx |
Approvals, supplements, products and documents come from FDA's Drugs@FDA data files, refreshed daily; Drugs@FDA lists approved applications only. Complete response letters are FDA's published letters. Drugs@FDA and FDA complete response letters
