FdaApplication
ANDA 206398
Identifiers
- fda_app_no: ANDA206398
Properties
| Property | Value |
|---|---|
| applicant_name | ALMAJECT INC |
| application_type | ANDA |
| approval_date | 2016-03-23 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| VORICONAZOLE | VORICONAZOLE | 200MG/VIAL | POWDER;INTRAVENOUS |
1 product