NDC 68001-186 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 68001-186 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA077690 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2014-03-01 |
| Marketing End Date | 2016-04-30 |