FdaApplication
NDA 019814
Identifiers
- fda_app_no: NDA019814
Properties
| Property | Value |
|---|---|
| applicant_name | ALLERGAN PHARMACEUTICAL |
| application_type | NDA |
| approval_date | 1989-06-28 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| BETAGAN | LEVOBUNOLOL HYDROCHLORIDE | 0.25% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | SOLUTION/DROPS;OPHTHALMIC |
1 product