FdaApplication
ANDA 075630
Identifiers
- fda_app_no: ANDA075630
Properties
| Property | Value |
|---|---|
| applicant_name | EUROFARMA INC |
| application_type | ANDA |
| approval_date | 2001-04-12 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| BETAXOLOL HYDROCHLORIDE | BETAXOLOL HYDROCHLORIDE | EQ 0.5% BASE | SOLUTION/DROPS;OPHTHALMIC |
1 product