FdaApplication
NDA 019383
Identifiers
- fda_app_no: NDA019383
Properties
| Property | Value |
|---|---|
| applicant_name | SCHERING CORP SUB SCHERING PLOUGH CORP |
| application_type | NDA |
| approval_date | 1987-07-13 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PROVENTIL | ALBUTEROL SULFATE | EQ 4MG BASE | TABLET, EXTENDED RELEASE;ORAL |
1 product