FdaApplication
NDA 009766
Identifiers
- fda_app_no: NDA009766
Properties
| Property | Value |
|---|---|
| applicant_name | SCHERING CORP SUB SCHERING PLOUGH CORP |
| application_type | NDA |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| METICORTEN | PREDNISONE | 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
| METICORTEN | PREDNISONE | 1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
2 products