NDC 55154-2356 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 55154-2356 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA087955 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2011-08-24 |
| Marketing End Date | 2013-07-31 |