FdaApplication
NDA 219868
Identifiers
- fda_app_no: NDA219868
Properties
| Property | Value |
|---|---|
| applicant_name | AZURITY PHARMACEUTICALS INC |
| application_type | NDA |
| approval_date | 2025-10-16 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| FERABRIGHT | FERUMOXYTOL | EQ 300MG IRON/10ML (EQ 30MG IRON/ML) | SOLUTION;INTRAVENOUS |
| FERABRIGHT | FERUMOXYTOL | EQ 510MG IRON/17ML (EQ 30MG IRON/ML) | SOLUTION;INTRAVENOUS |
2 products