FdaApplication
NDA 202429
Identifiers
- fda_app_no: NDA202429
Properties
| Property | Value |
|---|---|
| applicant_name | HOFFMANN LA ROCHE INC |
| application_type | NDA |
| approval_date | 2011-08-17 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ZELBORAF | VEMURAFENIB | 240MG | TABLET;ORAL |
1 product