NDC 0173-0661 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0173-0661 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA020977 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1998-12-29 |
| Marketing End Date | 2013-06-30 |
| Marketing Category | NDA |
| Application Number | NDA020977 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1998-12-29 |
| Marketing End Date | 2013-06-30 |