FdaApplication
NDA 216578
Identifiers
- fda_app_no: NDA216578
Properties
| Property | Value |
|---|---|
| applicant_name | ASTELLAS PHARMA US INC |
| application_type | NDA |
| approval_date | 2023-05-12 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| VEOZAH | FEZOLINETANT | 45MG | TABLET;ORAL |
1 product