NDC 42192-520 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 42192-520 |
| Marketing Category | / |
| Marketing Category | unapproved drug other |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2011-05-06 |
| Marketing End Date | 2013-10-31 |