FdaApplication
ANDA 074871
Identifiers
- fda_app_no: ANDA074871
Properties
| Property | Value |
|---|---|
| applicant_name | APOTEX INC |
| application_type | ANDA |
| approval_date | 1997-06-06 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| SELEGILINE HYDROCHLORIDE | SELEGILINE HYDROCHLORIDE | 5MG | TABLET;ORAL |
1 product