FdaApplication
NDA 018062
Identifiers
- fda_app_no: NDA018062
Properties
| Property | Value |
|---|---|
| applicant_name | SCHERING CORP SUB SCHERING PLOUGH CORP |
| application_type | NDA |
| approval_date | 1983-01-19 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PROVENTIL | ALBUTEROL SULFATE | EQ 2MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | SYRUP;ORAL |
1 product