FdaApplication
ANDA 080517
Identifiers
- fda_app_no: ANDA080517
Properties
| Property | Value |
|---|---|
| applicant_name | WATSON LABORATORIES INC |
| application_type | ANDA |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PREDNISOLONE SODIUM PHOSPHATE | PREDNISOLONE SODIUM PHOSPHATE | EQ 20MG PHOSPHATE/ML | INJECTABLE;INJECTION |
1 product