FdaApplication
ANDA 065011
Identifiers
- fda_app_no: ANDA065011
Properties
| Property | Value |
|---|---|
| applicant_name | FRESENIUS KABI USA LLC |
| application_type | ANDA |
| approval_date | 2000-07-03 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| CEFOXITIN | CEFOXITIN SODIUM | EQ 10GM BASE/VIAL | INJECTABLE;INJECTION |
1 product