FdaApplication
NDA 020333
Identifiers
- fda_app_no: NDA020333
Properties
| Property | Value |
|---|---|
| applicant_name | TAKEDA PHARMACEUTICALS USA INC |
| application_type | NDA |
| approval_date | 1997-03-14 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| AGRYLIN | ANAGRELIDE HYDROCHLORIDE | EQ 1MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | CAPSULE;ORAL |
| AGRYLIN | ANAGRELIDE HYDROCHLORIDE | EQ 0.5MG BASE | CAPSULE;ORAL |
2 products