FdaApplication
ANDA 078735
Identifiers
- fda_app_no: ANDA078735
Properties
| Property | Value |
|---|---|
| applicant_name | OXFORD PHARMACEUTICALS LLC |
| application_type | ANDA |
| approval_date | 2010-08-30 |
Products (5)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| SIMVASTATIN | SIMVASTATIN | 80MG | TABLET;ORAL |
| SIMVASTATIN | SIMVASTATIN | 5MG | TABLET;ORAL |
| SIMVASTATIN | SIMVASTATIN | 10MG | TABLET;ORAL |
| SIMVASTATIN | SIMVASTATIN | 40MG | TABLET;ORAL |
| SIMVASTATIN | SIMVASTATIN | 20MG | TABLET;ORAL |
5 products