NDC 58118-0019 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 58118-0019 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA050755 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2013-11-25 |
| Marketing End Date | 2016-08-08 |
| Marketing Category | ANDA |
| Application Number | ANDA050755 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2013-11-25 |
| Marketing End Date | 2016-08-08 |
| Marketing Category | ANDA |
| Application Number | ANDA050755 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2013-11-25 |
| Marketing End Date | 2016-08-08 |