NDC 58118-8947 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 58118-8947 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA074556 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2013-05-21 |
| Marketing End Date | 2014-09-01 |
| Marketing Category | ANDA |
| Application Number | ANDA074556 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2013-05-21 |
| Marketing End Date | 2017-06-15 |
| Marketing Category | ANDA |
| Application Number | ANDA074556 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2013-05-21 |
| Marketing End Date | 2014-09-01 |
| Marketing Category | ANDA |
| Application Number | ANDA074556 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2013-05-21 |
| Marketing End Date | 2014-09-01 |