FdaApplication
NDA 209661
Identifiers
- fda_app_no: NDA209661
Properties
| Property | Value |
|---|---|
| applicant_name | DUCHESNAY INC |
| application_type | NDA |
| approval_date | 2016-11-07 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| BONJESTA | DOXYLAMINE SUCCINATE; PYRIDOXINE HYDROCHLORIDE | 20MG;20MG | TABLET, EXTENDED RELEASE;ORAL |
1 product