NDC 55154-3350 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 55154-3350 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA076341 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2008-08-01 |
| Marketing End Date | 2015-11-30 |