NDC 0187-0791 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0187-0791 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA018602 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2010-12-25 |
| Marketing End Date | 2017-11-14 |