FdaApplication
NDA 022059
Identifiers
- fda_app_no: NDA022059
Properties
| Property | Value |
|---|---|
| applicant_name | NOVARTIS PHARMACEUTICALS CORP |
| application_type | NDA |
| approval_date | 2007-03-13 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| TYKERB | LAPATINIB DITOSYLATE | EQ 250MG BASE | TABLET;ORAL |
1 product