FdaApplication
NDA 020605
Identifiers
- fda_app_no: NDA020605
Properties
| Property | Value |
|---|---|
| applicant_name | SANDOZ INC |
| application_type | NDA |
| approval_date | 1997-01-24 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ZOFRAN | ONDANSETRON HYDROCHLORIDE | EQ 4MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | SOLUTION;ORAL |
1 product