NDC 0007-3163 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0007-3163 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA021410 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2003-10-13 |
| Marketing End Date | 2011-11-18 |
| Marketing Category | NDA |
| Application Number | NDA021410 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2009-07-16 |
| Marketing End Date | 2011-11-18 |