NDC 0173-0664 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0173-0664 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA020978 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1999-01-28 |
| Marketing End Date | 2012-10-31 |