FdaApplication
ANDA 205139
Identifiers
- fda_app_no: ANDA205139
Properties
| Property | Value |
|---|---|
| applicant_name | ACTAVIS LLC AN INDIRECT WHOLLY OWNED SUB OF TEVA PHARMACEUTICALS USA INC |
| application_type | ANDA |
| approval_date | 2017-12-08 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| BUSULFAN | BUSULFAN | 6MG/ML | INJECTABLE;INJECTION |
1 product