NDC 42808-101 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 42808-101 |
| Marketing Category | / |
| Marketing Category | unapproved drug other |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2011-08-01 |
| Marketing End Date | 2017-08-22 |