NDC 42769-1222 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 42769-1222 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA021519 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2008-01-25 |
| Marketing End Date | 2013-12-31 |