FdaApplication
NDA 019507
Identifiers
- fda_app_no: NDA019507
Properties
| Property | Value |
|---|---|
| applicant_name | SANOFI AVENTIS US LLC |
| application_type | NDA |
| approval_date | 1989-10-27 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| KERLONE | BETAXOLOL HYDROCHLORIDE | 20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
| KERLONE | BETAXOLOL HYDROCHLORIDE | 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
2 products