NDC 55154-6922 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 55154-6922 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA021366 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2010-12-01 |
| Marketing End Date | 2018-08-31 |
| Marketing Category | NDA |
| Application Number | NDA021366 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2010-12-01 |
| Marketing End Date | 2013-12-31 |
| Marketing Category | NDA |
| Application Number | NDA021366 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2010-12-01 |
| Marketing End Date | 2018-08-31 |