NDC 60258-850 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 60258-850 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA040644 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-06-15 |
| Marketing End Date | 2013-09-11 |
| Marketing Category | ANDA |
| Application Number | ANDA040644 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-06-15 |
| Marketing End Date | 2013-09-11 |