FdaApplication
ANDA 207609
Identifiers
- fda_app_no: ANDA207609
Properties
| Property | Value |
|---|---|
| applicant_name | SENTISS AG |
| application_type | ANDA |
| approval_date | 2019-04-17 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| LOTEPREDNOL ETABONATE | LOTEPREDNOL ETABONATE | 0.5% | SUSPENSION/DROPS;OPHTHALMIC |
1 product