NDC 0173-0742 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0173-0742 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA021652 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2004-08-18 |
| Marketing End Date | 2013-07-31 |