FdaApplication
NDA 020305
Identifiers
- fda_app_no: NDA020305
Properties
| Property | Value |
|---|---|
| applicant_name | HOFFMANN LA ROCHE INC |
| application_type | NDA |
| approval_date | 1995-03-16 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| KYTRIL | GRANISETRON HYDROCHLORIDE | EQ 2MG BASE **Federal Register determination that product was not withdrawn or discontinued for safety or effectiveness reasons** | TABLET;ORAL |
| KYTRIL | GRANISETRON HYDROCHLORIDE | EQ 1MG BASE **Federal Register determination that product was not withdrawn or discontinued for safety or effectiveness reasons** | TABLET;ORAL |
2 products