FdaApplication
NDA 018000
Identifiers
- fda_app_no: NDA018000
Properties
| Property | Value |
|---|---|
| applicant_name | SANOFI AVENTIS US LLC |
| application_type | NDA |
| approval_date | 1985-03-19 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| BRICANYL | TERBUTALINE SULFATE | 0.2MG/INH | AEROSOL, METERED;INHALATION |
1 product