NDC 58118-0184 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 58118-0184 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA077584 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2017-01-04 |
| Marketing End Date | 2018-12-01 |