FdaApplication
ANDA 070702
Identifiers
- fda_app_no: ANDA070702
Properties
| Property | Value |
|---|---|
| applicant_name | TEVA PHARMACEUTICALS USA INC |
| application_type | ANDA |
| approval_date | 1986-07-08 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| CLONIDINE HYDROCHLORIDE | CLONIDINE HYDROCHLORIDE | 0.2MG | TABLET;ORAL |
1 product