NDC 51862-140 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 51862-140 |
| Marketing Category | / |
| Marketing Category | Unapproved drug other |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2011-05-22 |
| Marketing End Date | 2014-04-30 |