FdaApplication
ANDA 077751
Identifiers
- fda_app_no: ANDA077751
Properties
| Property | Value |
|---|---|
| applicant_name | ZYDUS PHARMACEUTICALS USA INC |
| application_type | ANDA |
| approval_date | 2008-04-30 |
Products (4)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PRAVASTATIN SODIUM | PRAVASTATIN SODIUM | 80MG | TABLET;ORAL |
| PRAVASTATIN SODIUM | PRAVASTATIN SODIUM | 20MG | TABLET;ORAL |
| PRAVASTATIN SODIUM | PRAVASTATIN SODIUM | 40MG | TABLET;ORAL |
| PRAVASTATIN SODIUM | PRAVASTATIN SODIUM | 10MG | TABLET;ORAL |
4 products