FdaApplication
NDA 019046
Identifiers
- fda_app_no: NDA019046
Properties
| Property | Value |
|---|---|
| applicant_name | SCHERING CORP SUB SCHERING PLOUGH CORP |
| application_type | NDA |
| approval_date | 1987-04-06 |
Products (4)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| NORMOZIDE | HYDROCHLOROTHIAZIDE; LABETALOL HYDROCHLORIDE | 25MG;200MG | TABLET;ORAL |
| NORMOZIDE | HYDROCHLOROTHIAZIDE; LABETALOL HYDROCHLORIDE | 25MG;400MG | TABLET;ORAL |
| NORMOZIDE | HYDROCHLOROTHIAZIDE; LABETALOL HYDROCHLORIDE | 25MG;100MG | TABLET;ORAL |
| NORMOZIDE | HYDROCHLOROTHIAZIDE; LABETALOL HYDROCHLORIDE | 25MG;300MG | TABLET;ORAL |
4 products