FdaApplication
ANDA 211922
Identifiers
- fda_app_no: ANDA211922
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMACEUTICAL INDUSTRIES LTD |
| application_type | ANDA |
| approval_date | 2021-04-14 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| BUDESONIDE | BUDESONIDE | 0.25MG/2ML | SUSPENSION;INHALATION |
| BUDESONIDE | BUDESONIDE | 1MG/2ML | SUSPENSION;INHALATION |
| BUDESONIDE | BUDESONIDE | 0.5MG/2ML | SUSPENSION;INHALATION |
3 products