NDC 0062-0655 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0062-0655 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA021692 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2005-10-01 |
| Marketing End Date | 2011-10-31 |