FdaApplication
ANDA 040775
Identifiers
- fda_app_no: ANDA040775
Properties
| Property | Value |
|---|---|
| applicant_name | LANNETT CO INC |
| application_type | ANDA |
| approval_date | 2007-09-21 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PREDNISOLONE | PREDNISOLONE | 15MG/5ML | SOLUTION;ORAL |
1 product