FdaApplication
ANDA 205605
Identifiers
- fda_app_no: ANDA205605
Properties
| Property | Value |
|---|---|
| applicant_name | FRESENIUS KABI USA LLC |
| application_type | ANDA |
| approval_date | 2015-12-09 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| AMIKACIN SULFATE | AMIKACIN SULFATE | EQ 50MG BASE/ML | INJECTABLE;INJECTION |
1 product