FdaApplication
NDA 050622
Identifiers
- fda_app_no: NDA050622
Properties
| Property | Value |
|---|---|
| applicant_name | LEDERLE LABORATORIES DIV AMERICAN CYANAMID CO |
| application_type | NDA |
| approval_date | 1989-04-28 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| SUPRAX | CEFIXIME | 100MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | FOR SUSPENSION;ORAL |
1 product