FdaApplication
ANDA 214418
Identifiers
- fda_app_no: ANDA214418
Properties
| Property | Value |
|---|---|
| applicant_name | AUROLIFE PHARMA LLC |
| application_type | ANDA |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| BECLOMETHASONE DIPROPIONATE | BECLOMETHASONE DIPROPIONATE | 0.04MG/INH | AEROSOL, METERED;INHALATION |
| BECLOMETHASONE DIPROPIONATE | BECLOMETHASONE DIPROPIONATE | 0.08MG/INH | AEROSOL, METERED;INHALATION |
2 products