FdaApplication
ANDA 078988
Identifiers
- fda_app_no: ANDA078988
Properties
| Property | Value |
|---|---|
| applicant_name | PHARMACEUTICAL ASSOC INC |
| application_type | ANDA |
| approval_date | 2008-06-09 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PREDNISOLONE SODIUM PHOSPHATE | PREDNISOLONE SODIUM PHOSPHATE | EQ 20MG BASE/5ML | SOLUTION;ORAL |
1 product