NDC 0173-0721 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0173-0721 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA021548 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2003-11-06 |
| Marketing End Date | 2012-11-19 |