FdaApplication
ANDA 071865
Identifiers
- fda_app_no: ANDA071865
Properties
| Property | Value |
|---|---|
| applicant_name | USL PHARMA INC |
| application_type | ANDA |
| approval_date | 1987-09-09 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DESIPRAMINE HYDROCHLORIDE | DESIPRAMINE HYDROCHLORIDE | 50MG | TABLET;ORAL |
1 product