NDC 55154-4958 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 55154-4958 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA077795 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2007-10-09 |
| Marketing End Date | 2018-03-31 |