FdaApplication
NDA 019334
Identifiers
- fda_app_no: NDA019334
Properties
| Property | Value |
|---|---|
| applicant_name | QUAGEN PHARMACEUTICALS LLC |
| application_type | NDA |
| approval_date | 1989-06-05 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| SELEGILINE HYDROCHLORIDE | SELEGILINE HYDROCHLORIDE | 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
1 product