FdaApplication
ANDA 076097
Identifiers
- fda_app_no: ANDA076097
Properties
| Property | Value |
|---|---|
| applicant_name | APOTEX INC |
| application_type | ANDA |
| approval_date | 2002-02-06 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| CARTEOLOL HYDROCHLORIDE | CARTEOLOL HYDROCHLORIDE | 1% | SOLUTION/DROPS;OPHTHALMIC |
1 product