FdaApplication
NDA 219407
Identifiers
- fda_app_no: NDA219407
Properties
| Property | Value |
|---|---|
| applicant_name | IONIS PHARMACEUTICALS INC |
| application_type | NDA |
| approval_date | 2025-08-21 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DAWNZERA (AUTOINJECTOR) | DONIDALORSEN SODIUM | EQ 80MG BASE/0.8ML (EQ 80MG BASE/0.8ML) | SOLUTION;SUBCUTANEOUS |
1 product