FdaApplication
ANDA 072139
Identifiers
- fda_app_no: ANDA072139
Properties
| Property | Value |
|---|---|
| applicant_name | WARNER CHILCOTT DIV WARNER LAMBERT CO |
| application_type | ANDA |
| approval_date | 1988-06-13 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| CLONIDINE HYDROCHLORIDE | CLONIDINE HYDROCHLORIDE | 0.2MG | TABLET;ORAL |
1 product