FdaApplication
ANDA 208690
Identifiers
- fda_app_no: ANDA208690
Properties
| Property | Value |
|---|---|
| applicant_name | AMNEAL EU LTD |
| application_type | ANDA |
| approval_date | 2018-08-22 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DEXAMETHASONE SODIUM PHOSPHATE PRESERVATIVE FREE | DEXAMETHASONE SODIUM PHOSPHATE | EQ 10MG PHOSPHATE/ML | INJECTABLE;INJECTION |
1 product