NDC 0378-7065 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0378-7065 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA040569 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2009-11-02 |
| Marketing End Date | 2014-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA040569 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2009-11-02 |
| Marketing End Date | 2014-01-31 |