FdaApplication
NDA 021506
Identifiers
- fda_app_no: NDA021506
Properties
| Property | Value |
|---|---|
| applicant_name | ASTELLAS PHARMA US INC |
| application_type | NDA |
| approval_date | 2005-03-16 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| MYCAMINE | MICAFUNGIN SODIUM | EQ 50MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE;INTRAVENOUS |
| MYCAMINE | MICAFUNGIN SODIUM | EQ 100MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE;INTRAVENOUS |
2 products