FdaApplication
NDA 020363
Identifiers
- fda_app_no: NDA020363
Properties
| Property | Value |
|---|---|
| applicant_name | NOVARTIS PHARMACEUTICALS CORP |
| application_type | NDA |
| approval_date | 1994-06-29 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| FAMVIR | FAMCICLOVIR | 500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
| FAMVIR | FAMCICLOVIR | 125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
| FAMVIR | FAMCICLOVIR | 250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
3 products