FdaApplication
ANDA 065239
Identifiers
- fda_app_no: ANDA065239
Properties
| Property | Value |
|---|---|
| applicant_name | HIKMA FARMACEUTICA (PORTUGAL) SA |
| application_type | ANDA |
| approval_date | 2010-03-02 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| CEFOXITIN | CEFOXITIN SODIUM | EQ 10GM BASE/VIAL | INJECTABLE;INJECTION |
1 product