FdaApplication
ANDA 071588
Identifiers
- fda_app_no: ANDA071588
Properties
| Property | Value |
|---|---|
| applicant_name | ACTAVIS TOTOWA LLC |
| application_type | ANDA |
| approval_date | 1987-06-05 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DESIPRAMINE HYDROCHLORIDE | DESIPRAMINE HYDROCHLORIDE | 50MG | TABLET;ORAL |
1 product