FdaApplication
ANDA 202792
Identifiers
- fda_app_no: ANDA202792
Properties
| Property | Value |
|---|---|
| applicant_name | ACTAVIS ELIZABETH LLC AN INDIRECT WHOLLY OWNED SUB OF TEVA PHARMACEUTICALS USA INC |
| application_type | ANDA |
| approval_date | 2015-05-15 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| CLONIDINE HYDROCHLORIDE | CLONIDINE HYDROCHLORIDE | 0.1MG | TABLET, EXTENDED RELEASE;ORAL |
| CLONIDINE HYDROCHLORIDE | CLONIDINE HYDROCHLORIDE | 0.2MG | TABLET, EXTENDED RELEASE;ORAL |
2 products