NDC 55154-0673 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 55154-0673 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA071524 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2004-02-03 |
| Marketing End Date | 2015-10-31 |