FdaApplication
ANDA 076939
Identifiers
- fda_app_no: ANDA076939
Properties
| Property | Value |
|---|---|
| applicant_name | WATSON LABORATORIES INC |
| application_type | ANDA |
| approval_date | 2006-10-23 |
Products (4)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PRAVASTATIN SODIUM | PRAVASTATIN SODIUM | 40MG | TABLET;ORAL |
| PRAVASTATIN SODIUM | PRAVASTATIN SODIUM | 80MG | TABLET;ORAL |
| PRAVASTATIN SODIUM | PRAVASTATIN SODIUM | 10MG | TABLET;ORAL |
| PRAVASTATIN SODIUM | PRAVASTATIN SODIUM | 20MG | TABLET;ORAL |
4 products