FdaApplication
NDA 218395
Identifiers
- fda_app_no: NDA218395
Properties
| Property | Value |
|---|---|
| applicant_name | AZURITY PHARMACEUTICALS INC |
| application_type | NDA |
| approval_date | 2025-06-05 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| XIFYRM | MELOXICAM | 30MG/ML (30MG/ML) | SOLUTION;INTRAVENOUS |
1 product