NDC 0173-0714 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0173-0714 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA020564 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2002-09-25 |
| Marketing End Date | 2013-06-09 |