NDC 0781-7078 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0781-7078 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA077547 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | GM |
| Marketing Start Date | 2006-07-13 |
| Marketing End Date | 2015-06-30 |