FdaApplication
NDA 205108
Identifiers
- fda_app_no: NDA205108
Properties
| Property | Value |
|---|---|
| applicant_name | AZURITY PHARMACEUTICALS INC |
| application_type | NDA |
| approval_date | 2014-10-22 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| SOTYLIZE | SOTALOL HYDROCHLORIDE | 5MG/ML (5MG/ML) | SOLUTION;ORAL |
1 product