FdaApplication
ANDA 071252
Identifiers
- fda_app_no: ANDA071252
Properties
| Property | Value |
|---|---|
| applicant_name | INTERPHARM INC |
| application_type | ANDA |
| approval_date | 1986-10-01 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| CLONIDINE HYDROCHLORIDE | CLONIDINE HYDROCHLORIDE | 0.1MG | TABLET;ORAL |
1 product