NDC 58118-0159 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 58118-0159 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA075576 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2009-01-21 |
| Marketing End Date | 2017-02-22 |
| Marketing Category | ANDA |
| Application Number | ANDA075576 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2009-01-21 |
| Marketing End Date | 2017-02-22 |
| Marketing Category | ANDA |
| Application Number | ANDA075576 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2009-01-21 |
| Marketing End Date | 2017-02-22 |
| Marketing Category | ANDA |
| Application Number | ANDA075576 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2009-01-21 |
| Marketing End Date | 2017-02-22 |