FdaApplication
ANDA 075099
Identifiers
- fda_app_no: ANDA075099
Properties
| Property | Value |
|---|---|
| applicant_name | PHARMOBEDIENT CONSULTING |
| application_type | ANDA |
| approval_date | 2002-06-28 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PREDNISOLONE SODIUM PHOSPHATE | PREDNISOLONE SODIUM PHOSPHATE | EQ 5MG BASE/5ML | SOLUTION;ORAL |
1 product