NDC 60258-865 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 60258-865 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA079120 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2009-01-16 |
| Marketing End Date | 2013-09-11 |