FdaApplication
ANDA 209192
Identifiers
- fda_app_no: ANDA209192
Properties
| Property | Value |
|---|---|
| applicant_name | FRESENIUS KABI USA LLC |
| application_type | ANDA |
| approval_date | 2018-07-06 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DEXAMETHASONE SODIUM PHOSPHATE | DEXAMETHASONE SODIUM PHOSPHATE | EQ 10MG PHOSPHATE/ML | INJECTABLE;INJECTION |
1 product