FdaApplication
NDA 021908
Identifiers
- fda_app_no: NDA021908
Properties
| Property | Value |
|---|---|
| applicant_name | SUCAMPO PHARMA AMERICAS LLC |
| application_type | NDA |
| approval_date | 2006-01-31 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| AMITIZA | LUBIPROSTONE | 8MCG | CAPSULE;ORAL |
| AMITIZA | LUBIPROSTONE | 24MCG | CAPSULE;ORAL |
2 products