FdaApplication
NDA 018762
Identifiers
- fda_app_no: NDA018762
Properties
| Property | Value |
|---|---|
| applicant_name | NOVARTIS PHARMACEUTICALS CORP |
| application_type | NDA |
| approval_date | 1984-08-17 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| BRETHAIRE | TERBUTALINE SULFATE | 0.2MG/INH | AEROSOL, METERED;INHALATION |
1 product