FdaApplication
NDA 050715
Identifiers
- fda_app_no: NDA050715
Properties
| Property | Value |
|---|---|
| applicant_name | NOVARTIS PHARMACEUTICALS CORP |
| application_type | NDA |
| approval_date | 1995-07-14 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| NEORAL | CYCLOSPORINE | 25MG | CAPSULE;ORAL |
| NEORAL | CYCLOSPORINE | 100MG | CAPSULE;ORAL |
| NEORAL | CYCLOSPORINE | 50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | CAPSULE;ORAL |
3 products