FdaApplication
NDA 200603
Identifiers
- fda_app_no: NDA200603
Properties
| Property | Value |
|---|---|
| applicant_name | SUNOVION PHARMACEUTICALS INC |
| application_type | NDA |
| approval_date | 2010-10-28 |
Products (5)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| LATUDA | LURASIDONE HYDROCHLORIDE | 60MG | TABLET;ORAL |
| LATUDA | LURASIDONE HYDROCHLORIDE | 40MG | TABLET;ORAL |
| LATUDA | LURASIDONE HYDROCHLORIDE | 80MG | TABLET;ORAL |
| LATUDA | LURASIDONE HYDROCHLORIDE | 120MG | TABLET;ORAL |
| LATUDA | LURASIDONE HYDROCHLORIDE | 20MG | TABLET;ORAL |
5 products