NDC 68788-0008 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 68788-0008 |
| Marketing Category | / |
| Marketing Category | Unapproved drug other |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2010-12-18 |
| Marketing End Date | 2013-07-30 |