FdaApplication
ANDA 077126
Identifiers
- fda_app_no: ANDA077126
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMACEUTICAL INDUSTRIES LTD |
| application_type | ANDA |
| approval_date | 2008-03-14 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| AMIFOSTINE | AMIFOSTINE | 500MG/VIAL | INJECTABLE;INJECTION |
1 product