FdaApplication
NDA 021779
Identifiers
- fda_app_no: NDA021779
Properties
| Property | Value |
|---|---|
| applicant_name | ACTELION PHARMACEUTICALS US INC |
| application_type | NDA |
| approval_date | 2004-12-29 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| VENTAVIS | ILOPROST | 20MCG/ML (20MCG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | SOLUTION;INHALATION |
| VENTAVIS | ILOPROST | 10MCG/ML (10MCG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | SOLUTION;INHALATION |
| VENTAVIS | ILOPROST | 20MCG/2ML (10MCG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | SOLUTION;INHALATION |
3 products