FdaApplication
NDA 050589
Identifiers
- fda_app_no: NDA050589
Properties
| Property | Value |
|---|---|
| applicant_name | ASTELLAS PHARMA US INC |
| application_type | NDA |
| approval_date | 1984-10-03 |
Products (4)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| CEFIZOX IN DEXTROSE 5% IN PLASTIC CONTAINER | CEFTIZOXIME SODIUM | EQ 20MG BASE/ML | INJECTABLE;INJECTION |
| CEFIZOX IN DEXTROSE 5% IN PLASTIC CONTAINER | CEFTIZOXIME SODIUM | EQ 40MG BASE/ML | INJECTABLE;INJECTION |
| CEFIZOX IN PLASTIC CONTAINER | CEFTIZOXIME SODIUM | EQ 40MG BASE/ML | INJECTABLE;INJECTION |
| CEFIZOX IN PLASTIC CONTAINER | CEFTIZOXIME SODIUM | EQ 20MG BASE/ML | INJECTABLE;INJECTION |
4 products