FdaApplication
NDA 019807
Identifiers
- fda_app_no: NDA019807
Properties
| Property | Value |
|---|---|
| applicant_name | SANOFI AVENTIS US LLC |
| application_type | NDA |
| approval_date | 1992-10-30 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| KERLEDEX | BETAXOLOL HYDROCHLORIDE; CHLORTHALIDONE | 5MG;12.5MG | TABLET;ORAL |
| KERLEDEX | BETAXOLOL HYDROCHLORIDE; CHLORTHALIDONE | 10MG;12.5MG | TABLET;ORAL |
2 products