NDC 58657-401 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 58657-401 |
| Marketing Category | / |
| Marketing Category | UNAPPROVED DRUG OTHER |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2014-09-04 |
| Marketing End Date | 2017-11-20 |