FdaApplication
ANDA 076332
Identifiers
- fda_app_no: ANDA076332
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMACEUTICAL INDUSTRIES LTD |
| application_type | ANDA |
| approval_date | 2004-07-29 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| FLUCONAZOLE | FLUCONAZOLE | 200MG/5ML | FOR SUSPENSION;ORAL |
| FLUCONAZOLE | FLUCONAZOLE | 50MG/5ML | FOR SUSPENSION;ORAL |
2 products