FdaApplication
ANDA 075837
Identifiers
- fda_app_no: ANDA075837
Properties
| Property | Value |
|---|---|
| applicant_name | FRESENIUS KABI USA LLC |
| application_type | ANDA |
| approval_date | 2001-02-22 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| FLOXURIDINE | FLOXURIDINE | 500MG/VIAL | INJECTABLE;INJECTION |
1 product