NDC 55154-9359 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 55154-9359 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA017029 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2010-06-18 |
| Marketing End Date | 2013-06-30 |