FdaApplication
ANDA 078202
Identifiers
- fda_app_no: ANDA078202
Properties
| Property | Value |
|---|---|
| applicant_name | NEPHRON PHARMACEUTICALS CORPORATION |
| application_type | ANDA |
| approval_date | 2009-03-30 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| BUDESONIDE | BUDESONIDE | 0.25MG/2ML | SUSPENSION;INHALATION |
| BUDESONIDE | BUDESONIDE | 0.5MG/2ML | SUSPENSION;INHALATION |
2 products