NDC 58118-0042 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 58118-0042 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA079163 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2015-08-21 |
| Marketing End Date | 2018-10-23 |