FdaApplication
ANDA 064201
Identifiers
- fda_app_no: ANDA064201
Properties
| Property | Value |
|---|---|
| applicant_name | FRESENIUS KABI USA LLC |
| application_type | ANDA |
| approval_date | 2000-03-24 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| CEFOTAXIME | CEFOTAXIME SODIUM | EQ 20GM BASE/VIAL | INJECTABLE;INJECTION |
| CEFOTAXIME | CEFOTAXIME SODIUM | EQ 10GM BASE/VIAL | INJECTABLE;INJECTION |
2 products