FdaApplication
NDA 019059
Identifiers
- fda_app_no: NDA019059
Properties
| Property | Value |
|---|---|
| applicant_name | WYETH AYERST LABORATORIES |
| application_type | NDA |
| approval_date | 1985-07-03 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| INDERIDE LA 120/50 | HYDROCHLOROTHIAZIDE; PROPRANOLOL HYDROCHLORIDE | 50MG;120MG | CAPSULE, EXTENDED RELEASE;ORAL |
| INDERIDE LA 160/50 | HYDROCHLOROTHIAZIDE; PROPRANOLOL HYDROCHLORIDE | 50MG;160MG | CAPSULE, EXTENDED RELEASE;ORAL |
| INDERIDE LA 80/50 | HYDROCHLOROTHIAZIDE; PROPRANOLOL HYDROCHLORIDE | 50MG;80MG | CAPSULE, EXTENDED RELEASE;ORAL |
3 products