FdaApplication
ANDA 076417
Identifiers
- fda_app_no: ANDA076417
Properties
| Property | Value |
|---|---|
| applicant_name | WATSON LABORATORIES |
| application_type | ANDA |
| approval_date | 2005-04-18 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ANAGRELIDE HYDROCHLORIDE | ANAGRELIDE HYDROCHLORIDE | EQ 1MG BASE | CAPSULE;ORAL |
| ANAGRELIDE HYDROCHLORIDE | ANAGRELIDE HYDROCHLORIDE | EQ 0.5MG BASE | CAPSULE;ORAL |
2 products