Marketing-authorisation holder · United States
Eisai, Incorporated
15 medicines in 1 country, as authorisation holder.
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Marketing-authorisation holder · United States
15 medicines in 1 country, as authorisation holder.
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Every medicine in the registers under its name, current ones first.
15 medicines
| Medicine | Substance | Country | Status | Authorised |
|---|---|---|---|---|
| ARICEPT5mg/5ml · Solution | Donepezil | United States | Not marketed | 2004 |
| ARICEPT10mg | 23mg | 5mg · Tablet | Donepezil | United States | Marketed | 1996 |
| ARICEPT ODT10mg | 5mg · Tablet, orally disintegrating | Donepezil | United States | Not marketed | 2004 |
| BANZEL40mg/ml · Suspension | Rufinamide | United States | Marketed | 2011 |
| BANZEL100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | 200MG | 400MG · Tablet | Rufinamide | United States | Marketed | 2008 |
| DAYVIGO10mg | 5mg · Tablet | Lemborexant | United States | Marketed | 2019 |
| HALAVEN1mg/2ml (0.5mg/ml) · Solution | Eribulin | United States | Marketed | 2010 |
| HEXALEN50mg · Capsule | Altretamine | United States | Not marketed | 1990 |
| LENVIMA10mg base | 4mg base · Capsule | Lenvatinib | United States | Marketed | 2015 |
| LEQEMBI200mg/2ml | 500mg/5ml · Injectable | Lecanemab | United States | Marketed | 2023 |
| Leqembi IQLIK250mg/1.25ml (200mg/ml) · Injection | Lecanemab | United States | Marketed | 2026 |
| Leqembi IQLIK360mg/1.8ml (200mg/ml) · Injection | Lecanemab | United States | Marketed | 2025 |
| LEQEMBI IQLIK360mg/1.8ml(200mg/ml) · Injectable | Lecanemab | United States | Marketed | 2025 |
| LUSEDRA1050mg/30ml (35mg/ml) · Solution | Fospropofol | United States | Not marketed | 2008 |
| ONTAK150ug/ml · Vial | Denileukin diftitox | United States | Marketed | 1999 |
Where it holds or makes medicines, with how many are current.
| Country | Medicines | Current | Past | Companies |
|---|---|---|---|---|
| United States | 15 | 15 | 0 | CompaniesAll medicines |
The active substances in most of its medicines.
How the registers spell it, normalised: legal forms, accents and capitals removed.
Compiled by Prognia from the public medicine and company registers below. Logos are not used.
Source: U.S. FDA, Drugs@FDA / openFDA. FDA does not endorse this site.
Licence: Public domain (U.S. Government work)
FDA Purple Book, September 2026 release; acquired 2026-10-10T15:29:54.330165+00:00; exact source fields retained with source-key projections.
Licence: FDA-created structured factual administrative metadata; public-domain policy with third-party exceptions
Report an error or request removalCorrections from the company itself are welcome.
Other companies in the same group.
Ranked by their number of medicines.