FdaApplication
NDA 050791
Identifiers
- fda_app_no: NDA050791
Properties
| Property | Value |
|---|---|
| applicant_name | NOVARTIS PHARMACEUTICALS CORP |
| application_type | NDA |
| approval_date | 2004-02-27 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| MYFORTIC | MYCOPHENOLATE SODIUM | EQ 360MG BASE | TABLET, DELAYED RELEASE;ORAL |
| MYFORTIC | MYCOPHENOLATE SODIUM | EQ 180MG BASE | TABLET, DELAYED RELEASE;ORAL |
2 products