FdaApplication
NDA 205004
Identifiers
- fda_app_no: NDA205004
Properties
| Property | Value |
|---|---|
| applicant_name | FRESENIUS KABI USA LLC |
| application_type | NDA |
| approval_date | 2017-11-06 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| BORTEZOMIB | BORTEZOMIB | 3.5MG/VIAL | POWDER;INTRAVENOUS |
1 product