FdaApplication
ANDA 206220
Identifiers
- fda_app_no: ANDA206220
Properties
| Property | Value |
|---|---|
| applicant_name | MYLAN PHARMACEUTICALS INC |
| application_type | ANDA |
| approval_date | 2019-03-18 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| BEPOTASTINE BESILATE | BEPOTASTINE BESILATE | 1.5% | SOLUTION/DROPS;OPHTHALMIC |
1 product