FdaApplication
ANDA 078949
Identifiers
- fda_app_no: ANDA078949
Properties
| Property | Value |
|---|---|
| applicant_name | APOTEX INC |
| application_type | ANDA |
| approval_date | 2015-11-20 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| BUDESONIDE | BUDESONIDE | 0.032MG/INH | SPRAY, METERED;NASAL |
| BUDESONIDE | BUDESONIDE | 0.032MG/SPRAY | SPRAY, METERED;NASAL |
2 products