FdaApplication
ANDA 208158
Identifiers
- fda_app_no: ANDA208158
Properties
| Property | Value |
|---|---|
| applicant_name | BAUSCH AND LOMB INC |
| application_type | ANDA |
| approval_date | 2020-09-24 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ALAWAY | KETOTIFEN FUMARATE | EQ 0.025% BASE | SOLUTION/DROPS;OPHTHALMIC |
1 product