FdaApplication
ANDA 076056
Identifiers
- fda_app_no: ANDA076056
Properties
| Property | Value |
|---|---|
| applicant_name | AUROBINDO PHARMA USA INC |
| application_type | ANDA |
| approval_date | 2006-04-24 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PRAVASTATIN SODIUM | PRAVASTATIN SODIUM | 40MG | TABLET;ORAL |
| PRAVASTATIN SODIUM | PRAVASTATIN SODIUM | 10MG | TABLET;ORAL |
| PRAVASTATIN SODIUM | PRAVASTATIN SODIUM | 20MG | TABLET;ORAL |
3 products