FdaApplication
ANDA 065355
Identifiers
- fda_app_no: ANDA065355
Properties
| Property | Value |
|---|---|
| applicant_name | LUPIN PHARMACEUTICALS INC |
| application_type | ANDA |
| approval_date | 2007-04-10 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| SUPRAX | CEFIXIME | 200MG/5ML | FOR SUSPENSION;ORAL |
1 product