FdaApplication
NDA 213006
Identifiers
- fda_app_no: NDA213006
Properties
| Property | Value |
|---|---|
| applicant_name | SUMITOMO PHARMA AMERICA INC |
| application_type | NDA |
| approval_date | 2020-12-23 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| GEMTESA | VIBEGRON | 75MG | TABLET;ORAL |
1 product