FdaApplication
NDA 211929
Identifiers
- fda_app_no: NDA211929
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMACEUTICAL INDUSTRIES INC |
| application_type | NDA |
| approval_date | 2019-06-13 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ORTIKOS | BUDESONIDE | 6MG | CAPSULE, DELAYED RELEASE;ORAL |
| ORTIKOS | BUDESONIDE | 9MG | CAPSULE, DELAYED RELEASE;ORAL |
2 products