FdaApplication
NDA 216482
Identifiers
- fda_app_no: NDA216482
Properties
| Property | Value |
|---|---|
| applicant_name | AZURITY PHARMACEUTICALS INC |
| application_type | NDA |
| approval_date | 2024-05-01 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| MYHIBBIN | MYCOPHENOLATE MOFETIL | 200MG/ML | SUSPENSION;ORAL |
1 product