FdaApplication
ANDA 077122
Identifiers
- fda_app_no: ANDA077122
Properties
| Property | Value |
|---|---|
| applicant_name | IMPAX LABORATORIES INC |
| application_type | ANDA |
| approval_date | 2006-01-25 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DESMOPRESSIN ACETATE | DESMOPRESSIN ACETATE | 0.1MG | TABLET;ORAL |
| DESMOPRESSIN ACETATE | DESMOPRESSIN ACETATE | 0.2MG | TABLET;ORAL |
2 products