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Peganone (ETHOTOIN)
Peganone (ETHOTOIN) is an anti-epileptic agent developed by Recordati Rare, targeting the sodium channel alpha subunit. It is a small molecule modality approved by the FDA in 1957 for treating epilepsy characterized by intractable complex partial seizures and tonic-clonic epilepsy. Peganone is off-patent, with no active Orange Book patents, and no generic manufacturers. As an off-patent medication, its commercial status is subject to change. Key safety considerations are not explicitly stated in the provided facts.
At a glance
| Generic name | ETHOTOIN |
|---|---|
| Sponsor | Recordati |
| Drug class | Anti-epileptic Agent |
| Target | Sodium channel alpha subunit |
| Modality | Small molecule |
| Therapeutic area | Neuroscience |
| Phase | FDA-approved |
| First approval | 1957 |
Approved indications
- Epilepsy characterized by intractable complex partial seizures
- Tonic-clonic epilepsy
Common side effects
Drug interactions
- felodipine
- fluorouracil
- fluoxetine
- fluvoxamine
- phenytoin
Primary sources
Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.
| Source | Used for |
|---|---|
| FDA label | Mechanism, indications, dosing, boxed warnings, drug interactions |
Competitive intelligence
For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape:
- Peganone CI brief — competitive landscape report
- Peganone updates RSS · CI watch RSS
- Recordati portfolio CI