NDC 55154-5440 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 55154-5440 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA077857 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2010-07-23 |
| Marketing End Date | 2018-10-31 |