FdaApplication
NDA 019032
Identifiers
- fda_app_no: NDA019032
Properties
| Property | Value |
|---|---|
| applicant_name | PROMIUS PHARMA LLC |
| application_type | NDA |
| approval_date | 1986-10-27 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| TENEX | GUANFACINE HYDROCHLORIDE | EQ 3MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
| TENEX | GUANFACINE HYDROCHLORIDE | EQ 2MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
| TENEX | GUANFACINE HYDROCHLORIDE | EQ 1MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
3 products