NDC 54868-5489 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 54868-5489 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA020838 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2006-05-01 |
| Marketing End Date | 2011-06-30 |