FdaApplication
NDA 020225
Identifiers
- fda_app_no: NDA020225
Properties
| Property | Value |
|---|---|
| applicant_name | SCHERING PLOUGH CORP |
| application_type | NDA |
| approval_date | 1993-08-12 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| IMDUR | ISOSORBIDE MONONITRATE | 60MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET, EXTENDED RELEASE;ORAL |
| IMDUR | ISOSORBIDE MONONITRATE | 120MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET, EXTENDED RELEASE;ORAL |
| IMDUR | ISOSORBIDE MONONITRATE | 30MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET, EXTENDED RELEASE;ORAL |
3 products