FdaApplication
ANDA 209685
Identifiers
- fda_app_no: ANDA209685
Properties
| Property | Value |
|---|---|
| applicant_name | GLENMARK SPECIALTY SA |
| application_type | ANDA |
| approval_date | 2018-11-21 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ATOVAQUONE | ATOVAQUONE | 750MG/5ML | SUSPENSION;ORAL |
1 product