FdaApplication
NDA 012339
Identifiers
- fda_app_no: NDA012339
Properties
| Property | Value |
|---|---|
| applicant_name | SANOFI AVENTIS US LLC |
| application_type | NDA |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| BRONKOMETER | ISOETHARINE MESYLATE | 0.34MG/INH | AEROSOL, METERED;INHALATION |
| BRONKOSOL | ISOETHARINE HYDROCHLORIDE | 0.25% | SOLUTION;INHALATION |
| BRONKOSOL | ISOETHARINE HYDROCHLORIDE | 1% | SOLUTION;INHALATION |
3 products