NDC 0591-3171 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0591-3171 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA076768 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2008-08-04 |
| Marketing End Date | 2013-01-31 |