FdaApplication
NDA 203684
Identifiers
- fda_app_no: NDA203684
Properties
| Property | Value |
|---|---|
| applicant_name | BRACCO DIAGNOSTICS INC |
| application_type | NDA |
| approval_date | 2014-10-15 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| LUMASON | SULFUR HEXAFLUORIDE LIPID-TYPE A MICROSPHERES | 60.7MG/25MG | FOR SUSPENSION;INTRAVENOUS |
1 product