NDC 36000-028 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 36000-028 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA078084 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2008-11-20 |
| Marketing End Date | 2018-05-28 |