FdaApplication
NDA 022011
Identifiers
- fda_app_no: NDA022011
Properties
| Property | Value |
|---|---|
| applicant_name | NOVARTIS PHARMACEUTICALS CORP |
| application_type | NDA |
| approval_date | 2006-10-25 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| TYZEKA | TELBIVUDINE | 600MG | TABLET;ORAL |
1 product