FdaApplication
NDA 211810
Identifiers
- fda_app_no: NDA211810
Properties
| Property | Value |
|---|---|
| applicant_name | DAIICHI SANKYO INC |
| application_type | NDA |
| approval_date | 2019-08-02 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| TURALIO | PEXIDARTINIB HYDROCHLORIDE | EQ 125MG BASE | CAPSULE;ORAL |
| TURALIO | PEXIDARTINIB HYDROCHLORIDE | EQ 200MG BASE | CAPSULE;ORAL |
2 products