FdaApplication
NDA 206302
Identifiers
- fda_app_no: NDA206302
Properties
| Property | Value |
|---|---|
| applicant_name | ABBVIE INC |
| application_type | NDA |
| approval_date | 2016-06-03 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| BYVALSON | NEBIVOLOL HYDROCHLORIDE; VALSARTAN | EQ 5MG BASE;80MG | TABLET;ORAL |
1 product